Trial Outcomes & Findings for Comparison of Ultrasound Guided Versus Blind Corticosteroid Injection for Trochanteric Bursitis (NCT NCT02221817)
NCT ID: NCT02221817
Last Updated: 2021-10-20
Results Overview
COMPLETED
NA
80 participants
3 month
2021-10-20
Participant Flow
The study was ended and the PI has left the institution. The numbers presented are what was initially entered by the research team. From data available, 80 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 the 80 participants were enrolled in or if they completed the study.
Participant milestones
| Measure |
Blind
Trochanter injection
Trochanter bursa injections
|
Ultrasound
Trochanter injection
Trochanter bursa injections
Ultrasound
|
|---|---|---|
|
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
Comparison of Ultrasound Guided Versus Blind Corticosteroid Injection for Trochanteric Bursitis
Baseline characteristics by cohort
Baseline data not reported
PRIMARY outcome
Timeframe: 3 monthPopulation: The study was ended 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: Baseline, 2 weeks, 3 monthPopulation: The study was ended 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: 2 weeks, 3 monthPopulation: The study was ended 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: 2 weeks, 3 monthsPopulation: The study was ended 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.
Percent improvement
Outcome measures
Outcome data not reported
Adverse Events
Blind
Ultrasound
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