Trial Outcomes & Findings for Epidural Clonidine Versus Corticosteroid for Low Back Pain (NCT NCT02239627)
NCT ID: NCT02239627
Last Updated: 2021-01-20
Results Overview
TERMINATED
NA
16 participants
3 months
2021-01-20
Participant Flow
The study was terminated and the PI has left the institution. The numbers presented are what was initially entered by the research team. From data available, 16 participants were enrolled on the study; no information about those participants could be located. No other data could be located and it cannot be determined which arm the16 participants were enrolled in or if they completed the study.
Participant milestones
| Measure |
Steroid
Epidural steroid injection
Epidural steroid
|
Clonidine
Epidural clonidine injection
Clonidine
|
|---|---|---|
|
Overall Study
STARTED
|
0
|
0
|
|
Overall Study
COMPLETED
|
0
|
0
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Epidural Clonidine Versus Corticosteroid for Low Back Pain
Baseline characteristics by cohort
Baseline data not reported
PRIMARY outcome
Timeframe: 3 monthsPopulation: The study was terminated and the PI has left the institution. No results information is available, all efforts were to made to retrieve results information, but were unsuccessful. No study data is available.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Day 0, 3 weeks, 3 monthsPopulation: The study was terminated and the PI has left the institution. No results information is available, all efforts were to made to retrieve results information, but were unsuccessful. No study data is available.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 3 weeks, 3 monthsPopulation: The study was terminated and the PI has left the institution. No results information is available, all efforts were to made to retrieve results information, but were unsuccessful. No study data is available.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Day 0, 3 weeks, 3 monthsPopulation: The study was terminated and the PI has left the institution. No results information is available, all efforts were to made to retrieve results information, but were unsuccessful. No study data is available.
Outcome measures
Outcome data not reported
Adverse Events
Steroid
Clonidine
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Clinical Trials Compliance Coordinator
West Virginia Universtiy, WVCTSI
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place