Trial Outcomes & Findings for Detection of Borrelia Bacteria in Early Stage Lyme Borreliosis Using the T2Lyme Panel (NCT NCT03581279)
NCT ID: NCT03581279
Last Updated: 2022-02-04
Results Overview
Qualitative detection of genetic material (DNA) from the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as inclusive Borrelia spp.) from K2EDTA human whole blood samples using the T2Dx instrument and T2Lyme reagents.
TERMINATED
NA
18 participants
1 day
2022-02-04
Participant Flow
Participant milestones
| Measure |
EM Present
All patients must display signs/symptoms of Lyme disease as well as exhibit an EM lesion.
T2Lyme Panel testing: The T2Lyme Panel is an investigational use in vitro diagnostic (IVD) designed to qualitatively detect and identify the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as an inclusive Borrelia spp. detection channel) from K2EDTA human whole blood samples.
|
No EM Present
All patients must display signs/symptoms of Lyme disease but do not have an EM lesion.
T2Lyme Panel testing: The T2Lyme Panel is an investigational use in vitro diagnostic (IVD) designed to qualitatively detect and identify the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as an inclusive Borrelia spp. detection channel) from K2EDTA human whole blood samples.
|
|---|---|---|
|
Overall Study
STARTED
|
18
|
0
|
|
Overall Study
COMPLETED
|
16
|
0
|
|
Overall Study
NOT COMPLETED
|
2
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Detection of Borrelia Bacteria in Early Stage Lyme Borreliosis Using the T2Lyme Panel
Baseline characteristics by cohort
| Measure |
EM Present
n=18 Participants
All patients must display signs/symptoms of Lyme disease as well as exhibit an EM lesion.
T2Lyme Panel testing: The T2Lyme Panel is an investigational use in vitro diagnostic (IVD) designed to qualitatively detect and identify the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as an inclusive Borrelia spp. detection channel) from K2EDTA human whole blood samples.
|
No EM Present
All patients must display signs/symptoms of Lyme disease but do not have an EM lesion.
T2Lyme Panel testing: The T2Lyme Panel is an investigational use in vitro diagnostic (IVD) designed to qualitatively detect and identify the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as an inclusive Borrelia spp. detection channel) from K2EDTA human whole blood samples.
|
Total
n=18 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
|
8 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
8 Participants
n=206 Participants
|
|
Age, Categorical
>=65 years
|
10 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
10 Participants
n=206 Participants
|
|
Age, Continuous
|
66 years
STANDARD_DEVIATION 12 • n=99 Participants
|
—
|
66 years
STANDARD_DEVIATION 12 • n=206 Participants
|
|
Sex: Female, Male
Female
|
4 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
4 Participants
n=206 Participants
|
|
Sex: Female, Male
Male
|
14 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
14 Participants
n=206 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=99 Participants
|
—
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Asian
|
0 Participants
n=99 Participants
|
—
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=99 Participants
|
—
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Black or African American
|
0 Participants
n=99 Participants
|
—
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
White
|
0 Participants
n=99 Participants
|
—
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=99 Participants
|
—
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
18 Participants
n=99 Participants
|
—
|
18 Participants
n=206 Participants
|
|
Region of Enrollment
United States
|
18 participants
n=99 Participants
|
—
|
11 participants
n=206 Participants
|
PRIMARY outcome
Timeframe: 1 dayPopulation: The "No EM present" arm of the study was never initiated.
Qualitative detection of genetic material (DNA) from the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as inclusive Borrelia spp.) from K2EDTA human whole blood samples using the T2Dx instrument and T2Lyme reagents.
Outcome measures
| Measure |
EM Present
n=18 Participants
All patients must display signs/symptoms of Lyme disease as well as exhibit an EM lesion.
T2Lyme Panel testing: The T2Lyme Panel is an investigational use in vitro diagnostic (IVD) designed to qualitatively detect and identify the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as an inclusive Borrelia spp. detection channel) from K2EDTA human whole blood samples.
|
No EM Present
All patients must display signs/symptoms of Lyme disease but do not have an EM lesion.
T2Lyme Panel testing: The T2Lyme Panel is an investigational use in vitro diagnostic (IVD) designed to qualitatively detect and identify the major causative agents of Lyme disease (Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, as well as an inclusive Borrelia spp. detection channel) from K2EDTA human whole blood samples.
|
|---|---|---|
|
Number of Participants With Lyme Disease Detected in Human Whole Blood Samples
|
18 Participants
|
0 Participants
|
Adverse Events
EM Present
No EM Present
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Manager, Regulatory and Clinical Affairs
MDC Associates, Inc.
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place