Trial Outcomes & Findings for Central Nervous System Amplification in Lumbar Failed Back Surgery Syndrome (NCT NCT03444168)

NCT ID: NCT03444168

Last Updated: 2026-03-13

Results Overview

Measured by the Brief Pain Inventory (BPI). The BPI scores are a numerical rating scale and range from 0 to 10. A score of 0 is equal to no pain and a score of 10 is equal to pain as bad as you can imagine.

Recruitment status

COMPLETED

Target enrollment

158 participants

Primary outcome timeframe

Change from Baseline to Month 6

Results posted on

2026-03-13

Participant Flow

Participant milestones

Participant milestones
Measure
Candidate for Lumbar Spine Surgery
Participants have been designated to be a candidate for lumbar spine surgery to treat chronic low back and/or leg pain and you have agreed to proceed with the surgery.
Lumbar Failed Back Surgery Syndrome
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
Participants are a healthy volunteer wishing to participate in a research study.
Overall Study
STARTED
64
54
40
Overall Study
COMPLETED
55
49
40
Overall Study
NOT COMPLETED
9
5
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Central Nervous System Amplification in Lumbar Failed Back Surgery Syndrome

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Healthy Volunteer
n=40 Participants
Participants are a healthy volunteer with no chronic pain who are wishing to participate in a research study.
Total
n=144 Participants
Total of all reporting groups
Candidate for Lumbar Spine Surgery
n=55 Participants
Participants have been designated to be a candidate for lumbar spine surgery to treat chronic low back and/or leg pain and you have agreed to proceed with the surgery.
Lumbar Failed Back Surgery Syndrome
n=49 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Sex: Female, Male
Male
19 Participants
n=80 Participants
58 Participants
n=296 Participants
23 Participants
n=41 Participants
16 Participants
n=39 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
3 Participants
n=80 Participants
7 Participants
n=296 Participants
2 Participants
n=41 Participants
2 Participants
n=39 Participants
Age, Continuous
52 years
n=80 Participants
54 years
n=296 Participants
55 years
n=41 Participants
53 years
n=39 Participants
Sex: Female, Male
Female
21 Participants
n=80 Participants
86 Participants
n=296 Participants
32 Participants
n=41 Participants
33 Participants
n=39 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
37 Participants
n=80 Participants
137 Participants
n=296 Participants
53 Participants
n=41 Participants
47 Participants
n=39 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=80 Participants
0 Participants
n=296 Participants
0 Participants
n=41 Participants
0 Participants
n=39 Participants
Race/Ethnicity, Customized
Race · White
37 Participants
n=80 Participants
129 Participants
n=296 Participants
50 Participants
n=41 Participants
42 Participants
n=39 Participants
Race/Ethnicity, Customized
Race · Black, African American
1 Participants
n=80 Participants
8 Participants
n=296 Participants
4 Participants
n=41 Participants
3 Participants
n=39 Participants
Race/Ethnicity, Customized
Race · American Indian, Alaskan
0 Participants
n=80 Participants
1 Participants
n=296 Participants
0 Participants
n=41 Participants
1 Participants
n=39 Participants
Race/Ethnicity, Customized
Race · Asian
1 Participants
n=80 Participants
2 Participants
n=296 Participants
0 Participants
n=41 Participants
1 Participants
n=39 Participants
Race/Ethnicity, Customized
Race · Native Hawaiian or Pacific Islander
0 Participants
n=80 Participants
1 Participants
n=296 Participants
1 Participants
n=41 Participants
0 Participants
n=39 Participants
Race/Ethnicity, Customized
Race · Other, Unknown
1 Participants
n=80 Participants
3 Participants
n=296 Participants
0 Participants
n=41 Participants
2 Participants
n=39 Participants

PRIMARY outcome

Timeframe: Change from Baseline to Month 6

Population: Lumbar Spine Surgery Candidates (LSS) were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Only participants in the LSS group participated in longitudinal follow-up.

Measured by the Brief Pain Inventory (BPI). The BPI scores are a numerical rating scale and range from 0 to 10. A score of 0 is equal to no pain and a score of 10 is equal to pain as bad as you can imagine.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=21 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=31 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Clinical Pain Severity - 50% Reduction Responders vs Nonresponders
-83 percentage of change
Interval -100.0 to -62.5
0 percentage of change
Interval -12.5 to 15.5

PRIMARY outcome

Timeframe: Baseline

Population: Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. health surgery syndrome.

2011 Fibromyalgia Survey score is calculated by combining the widespread pain index (WPI) and the Symptom Severity Scale (SSI) to derive a score from 0-31. Scores greater than or equal to 13 indicate a diagnosis of Fibromyalgia. Higher scores indicate the degree of central sensitization present in a given individual.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=21 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=31 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=49 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=40 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Fibromylagia-ness (FMness)
FM Negative
17 Participants
27 Participants
26 Participants
40 Participants
Fibromylagia-ness (FMness)
FM positive
4 Participants
4 Participants
23 Participants
0 Participants

PRIMARY outcome

Timeframe: Baseline

Population: Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI.

PROMIS measures to be included are Depression, Anxiety, Physical Functioning, Fatigue, Sleep Impairment, Emotional Support, and Social Participation. Each questionnaire usually has 4-16 response options ranging in value from one to five. The total raw score for a short form with all questions answered is the sum of the values of the response to each question. The total range of potential raw scores depends on the number of questions being asked, for example, a 6 item form would have a range from is 6 to 30. After the raw score is calculated, a T-score metric is used to convert the raw score to a T-score. On the T-score metric, a score of 50 is the mean of a relevant reference population and 10 is the standard deviation of that mean. For PROMIS measures, higher scores equals "more of the concept being measured", this could be a desirable or undesirable outcome, depending on the concept being measured.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=21 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=31 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=49 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=40 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
PROMIS T-score - Fatigue, Physical Function, Sleep-Related Impairment
Fatigue v1.0 8a
58.80 units on a scale
Interval 51.4 to 64.4
56.40 units on a scale
Interval 48.1 to 61.5
62.40 units on a scale
Interval 57.1 to 66.1
42 units on a scale
Interval 33.1 to 47.7
PROMIS T-score - Fatigue, Physical Function, Sleep-Related Impairment
Physical Function v2.0 8b
34.70 units on a scale
Interval 31.8 to 36.3
35.30 units on a scale
Interval 30.4 to 40.6
34.30 units on a scale
Interval 32.0 to 36.3
60.10 units on a scale
Interval 52.8 to 60.1
PROMIS T-score - Fatigue, Physical Function, Sleep-Related Impairment
Sleep-Related Impairment v1.0 8a
60.90 units on a scale
Interval 52.5 to 66.0
59.70 units on a scale
Interval 50.5 to 62.9
62.30 units on a scale
Interval 53.1 to 66.1
44.60 units on a scale
Interval 38.4 to 50.3

PRIMARY outcome

Timeframe: Baseline

Population: 141 participants were analyzed at baseline. 3 participants did not have complete baseline data for these instruments and thus were not included in analysis. Lumbar Spine Surgery Pts were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Results were compared to the healthy controls and failed back surgery syndrome participants.

PROMIS measures to be included are Depression, Anxiety, Physical Functioning, Fatigue, Sleep Impairment, Emotional Support, and Social Participation. Each questionnaire usually has 4-16 response options ranging in value from one to five. The total raw score for a short form with all questions answered is the sum of the values of the response to each question. The total range of potential raw scores depends on the number of questions being asked, for example, a 6 item form would have a range from is 6 to 30. After the raw score is calculated, a T-score metric is used to convert the raw score to a T-score. On the T-score metric, a score of 50 is the mean of a relevant reference population and 10 is the standard deviation of that mean. For PROMIS measures, higher scores equals "more of the concept being measured", this could be a desirable or undesirable outcome, depending on the concept being measured.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=21 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=31 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=49 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=40 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
PROMIS T-score - Anxiety, Depression, Emotional Support, Pain Interference, Satisfaction With Social Roles
Anxiety v1.0 8a
50.3 units on a scale
Interval 44.0 to 61.0
49.8 units on a scale
Interval 43.9 to 54.6
51.00 units on a scale
Interval 45.9 to 60.1
43.35 units on a scale
Interval 37.1 to 50.6
PROMIS T-score - Anxiety, Depression, Emotional Support, Pain Interference, Satisfaction With Social Roles
Depression v1.0 8a
54.5 units on a scale
Interval 49.6 to 56.8
52.0 units on a scale
Interval 38.2 to 56.9
54.00 units on a scale
Interval 45.5 to 58.6
41.35 units on a scale
Interval 38.2 to 49.6
PROMIS T-score - Anxiety, Depression, Emotional Support, Pain Interference, Satisfaction With Social Roles
Emotional Support v2.0 4a
52.1 units on a scale
Interval 48.9 to 62.0
62.0 units on a scale
Interval 48.9 to 62.0
56.20 units on a scale
Interval 48.9 to 62.0
62.00 units on a scale
Interval 48.9 to 62.0
PROMIS T-score - Anxiety, Depression, Emotional Support, Pain Interference, Satisfaction With Social Roles
Pain Interference v2.0 8b
66.9 units on a scale
Interval 64.7 to 72.2
61.6 units on a scale
Interval 58.4 to 70.1
66.20 units on a scale
Interval 61.6 to 67.6
40.70 units on a scale
Interval 40.7 to 40.7
PROMIS T-score - Anxiety, Depression, Emotional Support, Pain Interference, Satisfaction With Social Roles
Satisfaction with Social Roles v1.0 4a
37.5 units on a scale
Interval 30.1 to 44.8
41.8 units on a scale
Interval 30.1 to 51.8
37.40 units on a scale
Interval 34.9 to 43.0
57.50 units on a scale
Interval 51.8 to 63.7

PRIMARY outcome

Timeframe: Baseline

Population: 141 pts were analyzed at baseline. Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Results were compared to the healthy controls and failed back surgery syndrome participants.

The Oswestry Disability Index will be used to assess low back pain. There are 10 sections on the index. Each section has a possible score of 5. The total possible range of scores is 0 to 50. A score of 0 indicates no pain. A score of 50 indicates the person is bed-bound or exaggerating their symptoms.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=21 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=31 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=49 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=40 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Oswestry Disability Index
42 units on a scale
Interval 32.0 to 54.0
40 units on a scale
Interval 28.0 to 58.0
44 units on a scale
Interval 38.0 to 56.0
1 units on a scale
Interval 0.0 to 3.0

SECONDARY outcome

Timeframe: Baseline

Population: Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Results were compared to the healthy controls and failed back surgery syndrome participants.

A 6-item catastrophizing scale that measures ways to cope or deal with pain. Each item is scored on a scale of 0-6. Scores can range from 0-36, with the higher the score the higher the rate of catastrophizing.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=21 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=31 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=49 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=40 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Coping Strategies Questionnaire - CAT
8 score on a scale
Interval 5.0 to 16.0
2 score on a scale
Interval 0.0 to 12.0
8 score on a scale
Interval 3.0 to 13.0
0.50 score on a scale
Interval 0.0 to 4.0

OTHER_PRE_SPECIFIED outcome

Timeframe: Baseline

Population: These numbers represent the subset of pts who participated in QST. Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Results were compared to the healthy controls and failed back surgery syndrome participants.

Pressure pain sensitivity is measured by Algometry (measured at the trapezius and lumbar spine). It yields a pressure pain threshold value measured in kPA. Tests were performed at the Left and Right trapezius in triplicate at each site and the average is calculated and used for analysis.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=4 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=7 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=22 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=29 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Algometry - Trapezius
Right Trapezius
299.7 kPA
Interval 197.8 to 381.7
263.7 kPA
Interval 171.7 to 349.0
251.5 kPA
Interval 198.3 to 309.0
285.7 kPA
Interval 213.3 to 331.0
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Algometry - Trapezius
Left Trapezius
287.2 kPA
Interval 209.8 to 377.7
303.7 kPA
Interval 208.3 to 352.3
227.3 kPA
Interval 175.3 to 310.3
280.3 kPA
Interval 212.0 to 368.7

OTHER_PRE_SPECIFIED outcome

Timeframe: Baseline

Population: A subset of participants completed QST measure at baseline. Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Results were compared to the healthy controls and failed back surgery syndrome participants.

Pressure pain sensitivity is measured by Algometry (measured at the trapezius and lumbar spine). It yields a pressure pain threshold value measured in kPA.Tests were performed at the Left and Right lumbar spine in triplicate at each site and the average is calculated and used for analysis.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=4 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=6 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=22 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=29 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Algometry - Lower Back
Left Back
342.3 kPA
Interval 178.2 to 456.5
291.5 kPA
Interval 196.7 to 341.0
221.3 kPA
Interval 108.3 to 363.0
332.7 kPA
Interval 297.0 to 403.7
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Algometry - Lower Back
Right Back
344.2 kPA
Interval 188.0 to 437.0
328 kPA
Interval 168.3 to 413.0
173.3 kPA
Interval 145.7 to 318.3
321.0 kPA
Interval 274.0 to 433.3

OTHER_PRE_SPECIFIED outcome

Timeframe: Baseline

Population: A subset of participants completed QST measure at baseline. Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Results were compared to the healthy controls and failed back surgery syndrome participants.

Pressure pain sensitivity is measured by the Multimodal Automated Sensory Testing (MAST) System (measured at the thumbnail). It yields a pressure pain threshold value measured in kg/cm2. Thumb Pain30, Pain40, and Pain50 are the pressure intensities that provoke a pain rating of 30/100, 40/100, and 50/100, respectively. Thumb Pain Tolerance is the pressure intensity that provokes a response greater than or equal to 80/100.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=4 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=8 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=29 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=22 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Multimodal Automated Sensory Testing
Thumb Pain30
3.86 kg/cm^2
Interval 2.66 to 4.37
3.69 kg/cm^2
Interval 2.72 to 5.33
3.0 kg/cm^2
Interval 2.0 to 3.7
4.0 kg/cm^2
Interval 3.1 to 5.0
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Multimodal Automated Sensory Testing
Thumb Pain40
4.60 kg/cm^2
Interval 3.26 to 5.08
4.01 kg/cm^2
Interval 2.74 to 5.88
3.6 kg/cm^2
Interval 2.5 to 4.2
4.6 kg/cm^2
Interval 3.7 to 5.4
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Multimodal Automated Sensory Testing
Thumb Pain50
5.35 kg/cm^2
Interval 3.86 to 5.78
4.23 kg/cm^2
Interval 3.31 to 6.52
4.0 kg/cm^2
Interval 2.8 to 4.6
5.3 kg/cm^2
Interval 4.1 to 5.9
Quantitative Sensory Testing (QST) - Pressure Pain Sensitivity by Multimodal Automated Sensory Testing
Thumb Pain Tolerance
7.50 kg/cm^2
Interval 5.65 to 7.89
4.98 kg/cm^2
Interval 4.13 to 8.47
5.6 kg/cm^2
Interval 4.8 to 6.2
6.6 kg/cm^2
Interval 5.7 to 7.9

OTHER_PRE_SPECIFIED outcome

Timeframe: Change from Post-stimulus test at Baseline visit to Pre-stimulus test at Baseline visit

Population: A subset of participants completed QST measure at baseline. Lumbar Spine Surgery Candidates were asked BPI prior to surgery (baseline) and 6 months post surgery. Based on this response, participants were split in to two groups, responders vs non-responders. Responders were defined as patients who reported a \>50% reduction in pain on the BPI. Results were compared to the healthy controls and failed back surgery syndrome participants.

Conditioned Pain Modulation as measured at the thumbnail using the MAST. It yields a numerical pain rating difference on a 0-100 numerical scale that can either be positive or negative called CPM magnitude. CPM magnitude will be calculated as the difference (post-pre) in the mean of the three pain ratings given to the test stimulus prior to the conditioning stimuli and the three pain ratings of the test stimulus given during the conditioning stimuli. A reduction in test stimulus rating by conditioning stimulation implies functional (inhibitory) CPM, and the degree of reduction expresses the efficiency of CPM.

Outcome measures

Outcome measures
Measure
Lumbar Spine Surgery - Responders
n=3 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a greater than 50% reduction in pain BPI between baseline and 6 months.
Lumbar Spine Surgery - Non-Responders
n=7 Participants
Participants who received lumbar spine surgery to treat chronic low back and/or leg pain and have reported a less than 50% reduction in pain BPI between baseline and 6 months
Lumbar Failed Back Surgery Syndrome
n=21 Participants
Participants have been diagnosed with having lumbar failed back surgery syndrome and have persistent and moderate-to-severe low back and/or leg pain for more than 6 months after a lumbar spine surgery.
Healthy Volunteer
n=29 Participants
Participants are a healthy volunteer with no chronic pain wishing to participate in a research study.
Quantitative Sensory Testing (QST) - Conditioned Pain Modulation (CPM)
-3.33 units on a scale
Interval -13.33 to 1.67
-1.67 units on a scale
Interval -15.0 to 1.67
-5.0 units on a scale
Interval -15.0 to 0.0
-1.7 units on a scale
Interval -8.3 to 3.3

Adverse Events

Lumbar Spine Surgery Candidates

Serious events: 1 serious events
Other events: 0 other events
Deaths: 1 deaths

Healthy Control Participants

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Failed Back Surgery Syndrome Participants

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
Lumbar Spine Surgery Candidates
n=55 participants at risk
Participants have been designated to be a candidate for lumbar spine surgery to treat chronic low back and/or leg pain and you have agreed to proceed with the surgery.
Healthy Control Participants
n=40 participants at risk
Patients with no chronic pain who were not undergoing a lumbar spine surgery.
Failed Back Surgery Syndrome Participants
n=49 participants at risk
Participants who had a lumbar spine surgery procedure and still reported moderate to severe lower back pain.
General disorders
Death
1.8%
1/55 • Number of events 1 • AEs were assessed via pt-report or via EMR notification for the duration of the study, approximately 6 months.
0.00%
0/40 • AEs were assessed via pt-report or via EMR notification for the duration of the study, approximately 6 months.
0.00%
0/49 • AEs were assessed via pt-report or via EMR notification for the duration of the study, approximately 6 months.

Other adverse events

Adverse event data not reported

Additional Information

Dr. Andrea Chadwick

The University of Kansas Medical Center

Phone: 913-588-3479

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place