Trials / Completed
CompletedNCT03120923
Combined Corticosteroid With Low Volume Compared to High Volume in Impingement Syndrome
A Short Term Outcomes of Subacromial Injection of Combined Corticosteroid With Low Volume Compared to High Volume of Local Anesthetic for Rotator Cuff Impingement Syndrome: A Randomized Controlled Trials
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 52 (actual)
- Sponsor
- Ramathibodi Hospital · Academic / Other
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to assess and compare the effectiveness of two different volumes of local anesthetic combined with 40mg of triamcinolone for subacromial injections in treating patients with rotator cuff impingement syndrome
Detailed description
Patients with rotator cuff impingement syndrome were randomized to undergo subacromial injection with 10mL total volume of 1% lidocaine plus 40mg triamcinolone acetonide (n = 22), or a 4mL total volume of 1% lidocaine plus 40-mg triamcinolone acetonide (n = 23). Evaluations using a visual analog scale (VAS) for pain during motion, and the Western Ontario Rotator Cuff Index (WORC) were completed before treatment and 30 minutes, 2 weeks, and 8 weeks after injection.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine 3 cc | |
| DRUG | Lidocaine 9 cc | 9mL of 1% lidocaine plus 1mL of 40mg triamcinolone acetonide |
| DRUG | Triamcinolone Acetonide |
Timeline
- Start date
- 2015-01-01
- Primary completion
- 2016-08-01
- Completion
- 2016-08-01
- First posted
- 2017-04-19
- Last updated
- 2017-10-18
Source: ClinicalTrials.gov record NCT03120923. Inclusion in this directory is not an endorsement.