Trials / Withdrawn
WithdrawnNCT05364099
Suprascapular Nerve Block for Treatment of Shoulder Pain in Individuals With Spinal Cord Injuries
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- University of Miami · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the effectiveness and safety of using suprascapular nerve block for individuals with chronic spinal cord injury who have chronic shoulder pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine 1% Injectable Solution | 2.5 ml of 1% Lidocaine will be administered via injection in suprascapular nerve in the suprascapular notch |
| DRUG | Triamcinolone Injection | 0.5 ml 40mg/ml Triamcinolone will be administered via injection in suprascapular nerve in the suprascapular notch |
| PROCEDURE | Suprascapular Nerve Block | This procedure involves injection of a lidocaine and triamcinolone mixture into the suprascapular nerve in the suprascapular notch using ultrasound guidance for proper placement of drugs. |
Timeline
- Start date
- 2023-11-27
- Primary completion
- 2024-01-01
- Completion
- 2024-01-01
- First posted
- 2022-05-06
- Last updated
- 2023-12-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05364099. Inclusion in this directory is not an endorsement.