Trial Outcomes & Findings for Efficacy Study of Amantadine to Treat Gait Dysfunction and Freezing in Parkinson's Disease (NCT NCT01652534)

NCT ID: NCT01652534

Last Updated: 2019-11-13

Results Overview

This is a walking assessment. The subject will begin in the seated position, stand up, walk 7 meters, turn around, and sit back down. The entire process from leaving the chair to returning to the chair will be timed. Also, the Timed Up and Go (TUG) will be done both in the ON and OFF states.

Recruitment status

TERMINATED

Study phase

PHASE3

Target enrollment

3 participants

Primary outcome timeframe

Baseline, change at 4 weeks

Results posted on

2019-11-13

Participant Flow

There was a total of 3 participants enrolled into the study. All 3 participants were randomized to receive either Amantadine or Placebo and crossed over after a washout period.

Participant milestones

Participant milestones
Measure
Amantadine, Then Placebo
Participants first received Amantadine 100 mg tablet orally once a day for one week, then two tablets orally twice a day for one week. After a washout period of 3 weeks, they then placebo tablet (matching Amantadine 100mg tablet) orally for 4 weeks.
Placebo, Then Amantadine
Participants first received Placebo tablet (matching Amantadine 100 mg tablet) orally once a day for one week, then Amantadine placebo two tablets orally twice a day for one week. After a washout period of 4 weeks, then they received Amantadine 100mg tablet orally for 4 weeks.
Overall Study
STARTED
2
1
Overall Study
COMPLETED
1
1
Overall Study
NOT COMPLETED
1
0

Reasons for withdrawal

Reasons for withdrawal
Measure
Amantadine, Then Placebo
Participants first received Amantadine 100 mg tablet orally once a day for one week, then two tablets orally twice a day for one week. After a washout period of 3 weeks, they then placebo tablet (matching Amantadine 100mg tablet) orally for 4 weeks.
Placebo, Then Amantadine
Participants first received Placebo tablet (matching Amantadine 100 mg tablet) orally once a day for one week, then Amantadine placebo two tablets orally twice a day for one week. After a washout period of 4 weeks, then they received Amantadine 100mg tablet orally for 4 weeks.
Overall Study
Lack of Efficacy
1
0

Baseline Characteristics

Efficacy Study of Amantadine to Treat Gait Dysfunction and Freezing in Parkinson's Disease

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Amantadine Crossover to Placebo
n=2 Participants
For first 4 weeks of study Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN). Crossover to Placebo (sugar pill) at week 7
Placebo Crossover to Amantadine
n=1 Participants
For first 4 weeks of study, Placebo (sugar pill) Crossover to Amantadine at week 7 Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Total
n=3 Participants
Total of all reporting groups
Age, Categorical
<=18 years
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Age, Categorical
>=65 years
2 Participants
n=99 Participants
1 Participants
n=107 Participants
3 Participants
n=206 Participants
Sex: Female, Male
Female
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Sex: Female, Male
Male
2 Participants
n=99 Participants
1 Participants
n=107 Participants
3 Participants
n=206 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race (NIH/OMB)
Asian
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race (NIH/OMB)
Black or African American
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race (NIH/OMB)
White
2 Participants
n=99 Participants
1 Participants
n=107 Participants
3 Participants
n=206 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Region of Enrollment
United States
2 participants
n=99 Participants
1 participants
n=107 Participants
3 participants
n=206 Participants

PRIMARY outcome

Timeframe: Baseline, change at 4 weeks

Population: participants who could complete the task. Note: for the 2 participants who were tested while on placebo, one did not complete baseline, and one did not complete week 4, so a change could not be computed.

This is a walking assessment. The subject will begin in the seated position, stand up, walk 7 meters, turn around, and sit back down. The entire process from leaving the chair to returning to the chair will be timed. Also, the Timed Up and Go (TUG) will be done both in the ON and OFF states.

Outcome measures

Outcome measures
Measure
Amantadine
n=3 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=1 Participants
Sugar Pill Placebo: Sugar Pill
Timed Up and Go (TUG) - ON Usual Medication
Baseline
16.7 seconds
Interval 15.86 to 18.16
17.4 seconds
Interval 17.4 to 17.4
Timed Up and Go (TUG) - ON Usual Medication
Change at 4 weeks
0.04 seconds
Interval -0.8 to 1.45

PRIMARY outcome

Timeframe: Baseline, change at 4 weeks

Population: participants who could complete the task.

This is a walking assessment. The subject will begin in the seated position, stand up, walk 7 meters, turn around, and sit back down. The entire process from leaving the chair to returning to the chair will be timed. Also, the Timed Up and Go (TUG) will be done both in the ON and OFF states.

Outcome measures

Outcome measures
Measure
Amantadine
n=2 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=2 Participants
Sugar Pill Placebo: Sugar Pill
Timed Up and Go (TUG) - OFF Usual Medication
Baseline
23 seconds
Interval 20.0 to 24.0
19.5 seconds
Interval 17.0 to 22.0
Timed Up and Go (TUG) - OFF Usual Medication
Change at 4 weeks
-3.5 seconds
Interval -4.3 to -2.7
8.6 seconds
Interval -0.2 to 17.5

SECONDARY outcome

Timeframe: Baseline, change in 4 weeks

Population: participants who completed task

The subject sits in the chair approximately 3 1/2 meters away from doorway with the door closed. Subject then stands up and walks one meter to a 40cm X 40cm box taped on the floor. Within the box the patient turns clockwise (360 degrees), then turns counterclockwise (360 degrees). Walk to open the door and walk through the doorway, turn around and return to the chair. Modified Timed Up and Go (mTUG) completed in three components including walking the course without additional tasks, carrying a tray with a cup of water, and counting backwards from 100, in both ON and OFF state.

Outcome measures

Outcome measures
Measure
Amantadine
n=1 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=1 Participants
Sugar Pill Placebo: Sugar Pill
Modified Timed Up and Go (mTUG)
Baseline - ON
14 seconds
Standard Deviation 0
16 seconds
Standard Deviation 0
Modified Timed Up and Go (mTUG)
change in 4 weeks - ON
1 seconds
Standard Deviation 0
-1 seconds
Standard Deviation 0
Modified Timed Up and Go (mTUG)
Baseline - OFF
16 seconds
Standard Deviation 0
20 seconds
Standard Deviation 0
Modified Timed Up and Go (mTUG)
change in 4 weeks - OFF
2 seconds
Standard Deviation 0
1 seconds
Standard Deviation 0

SECONDARY outcome

Timeframe: Baseline, change in 4 weeks

Population: patients who report being ON and OFF medication and experience dyskinesia under either condition at baseline and after 4 weeks of either Amantadine or Placebo. NOTE: only one patient reported both dyskinesia at baseline and 4 weeks and only under the placebo condition. Others did not report any OFF time, so the difference could not be calculated.

Subject will record motor activity as OFF, ON (mobility improved) or asleep on the diary every half hour for two days. Subjects further define ON time according to dyskinesia categories "none", "non-troublesome" or "troublesome." The home diaries are used as an evaluation measure of the intervention by assessing the change in off time and change in on time with troublesome dyskinesia. The difference in time experiencing dyskinesia while ON meds relative to the time OFF meds at baseline and at 4 weeks is compared.

Outcome measures

Outcome measures
Measure
Amantadine
n=1 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=1 Participants
Sugar Pill Placebo: Sugar Pill
Analysis of Motor Functioning Using the Parkinson's Home Diaries
Baseline
90 minutes
Standard Deviation 0
150 minutes
Standard Deviation 0
Analysis of Motor Functioning Using the Parkinson's Home Diaries
Change at 4 weeks
450 minutes
Standard Deviation 0

SECONDARY outcome

Timeframe: Baseline, change in 4 weeks

Population: Participants who completed questionnaire

A questionnaire that is used to assess the likelihood of the subject freezing in a number of different scenarios. 0=No freezing of gait to 24=severe freezing of gait

Outcome measures

Outcome measures
Measure
Amantadine
n=3 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=2 Participants
Sugar Pill Placebo: Sugar Pill
Freezing of Gait Questionnaire
Baseline
10 score on a scale
Interval 9.0 to 17.0
15 score on a scale
Interval 13.0 to 17.0
Freezing of Gait Questionnaire
Change at 4 weeks
-2 score on a scale
Interval -7.0 to 3.0
1 score on a scale
Interval -1.0 to 3.0

SECONDARY outcome

Timeframe: 4 weeks

Population: number completing study up to assessment

Global Improvement is the second scale in the clinical global impression (CGI). Total overall improvement is judged by whether or not, in the judgment of the assessor, the improvement is entirely due to the drug treatment. It is also a 1-7 point weighted scale, going from "very much improved" (1) to "very much worse" (7). A zero score is assigned if the score is not assessed.

Outcome measures

Outcome measures
Measure
Amantadine
n=3 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=2 Participants
Sugar Pill Placebo: Sugar Pill
Clinical Global Impression (CGI)
2 score on a scale
Interval 2.0 to 6.0
4.5 score on a scale
Interval 4.0 to 5.0

SECONDARY outcome

Timeframe: Baseline, week 4

Population: Participants completing questionnaire

The Parkinson's Disease Questionnaire-39 (PDQ39) is a copyrighted instrument to assess symptoms of Parkinson's disease (PD) with 39 questions relating to mobility, activities of daily living, emotional well-being, social support, cognition, communication and bodily discomfort. The test asks subjects to rate each question regarding their Parkinson's disease symptoms over the past month. (range 0 to 100, lower scores reflect better quality of life)

Outcome measures

Outcome measures
Measure
Amantadine
n=2 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
Sugar Pill Placebo: Sugar Pill
Parkinson's Disease Questionnaire-39 (PDQ-39)
Baseline
38 score on a scale
Interval 32.0 to 43.0

SECONDARY outcome

Timeframe: Baseline, week 4, week 7, week 11

Population: No data was collected from the portable devices that were used.

Use of an accelerometer such as Motorola Droid and wireless acceleration sensors to record gait parameters step time, walking speed, and cadence during the timed up and go (TUG) and modified timed up and go (mTUG) components. The sensors will be attached to the subject's legs and trunk using Velcro straps. The accelerometer will be held or clipped onto the subject in order to measure his or her acceleration. This is done within clinic and during the visit time.

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: Baseline, change in 4 weeks

Population: Participants who completed questionnaire

A questionnaire used to discriminate between Parkinson Disease (PD) patients with fatigue and those without fatigue. Range 9 to 63, higher scores indicate greater fatigue severity.

Outcome measures

Outcome measures
Measure
Amantadine
n=2 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=2 Participants
Sugar Pill Placebo: Sugar Pill
Fatigue Severity Scale (FSS)
Baseline
27 score on a scale
Interval 13.0 to 32.0
26 score on a scale
Interval 12.0 to 40.0
Fatigue Severity Scale (FSS)
change in 4 weeks
1.5 score on a scale
Interval 0.0 to 3.0
-5 score on a scale
Interval -10.0 to 0.0

SECONDARY outcome

Timeframe: week 4

Population: participants who completed study to time of assessment

Tolerability analysis as determined by the number of subjects completing each arm of the study.

Outcome measures

Outcome measures
Measure
Amantadine
n=3 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=2 Participants
Sugar Pill Placebo: Sugar Pill
Number Who Completed Medication as Randomized
3 Participants
2 Participants

SECONDARY outcome

Timeframe: Week 4

Analyzing the safety of the medication, Amantadine. Data regarding the medication will be collected from the patient on each visit including any adverse events since the last visit, frequency and severity of falls. This is done in order to determine the safety of Amantadine.

Outcome measures

Outcome measures
Measure
Amantadine
n=3 Participants
Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day Amantadine: Amantadine 100mg daily, for a week, if it is tolerated Amantadine will increase to 1 tab twice a day. Amantadine will then be administered orally twice daily in the morning with breakfast and at noon with lunch (AM and NN).
Placebo
n=2 Participants
Sugar Pill Placebo: Sugar Pill
Number of Participants With Drug Safety Reports
0 Participants
0 Participants

Adverse Events

Amantadine

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

Placebo

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

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr. Tanya Simuni

Northwestern University

Phone: 312-503-2970

Results disclosure agreements

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