Trials / Terminated
TerminatedNCT04126278
Calcific Tendonitis Treatment: Barbotage vs. Barbotage With Cortisone Injection
Calcific Tendonitis Treatment: Barbotage vs. Barbotage With Cortisone Injection: A Randomized Controlled Double-Blind Study
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 4 (actual)
- Sponsor
- NYU Langone Health · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the efficacy of barbotage therapy by comparing the clinical and sonographic changes in patients that solely receive barbotage to patients receiving the standard of care, barbotage with cortisone injection.
Detailed description
Calcific tendonitis is a condition caused by calcium deposits building up in a person's muscles or tendons. If calcium builds up in an area, a person may feel pain and discomfort there. The purpose of this study is to determine the efficacy of barbotage therapy (injecting and washing the shoulder joint with saline) by comparing the amount of pain, shoulder function, and X-Rays in patients with calcific tendonitis that receive the standard of care, barbotage with cortisone injection, against barbotage with saline injection. Receiving barbotage without cortisone is therefore considered experimental.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Barbotage | Administered as per standard of care |
| DRUG | Dexamethasone | 4 mg of dexamethasone |
Timeline
- Start date
- 2020-12-01
- Primary completion
- 2022-08-12
- Completion
- 2022-08-23
- First posted
- 2019-10-15
- Last updated
- 2024-01-05
- Results posted
- 2024-01-05
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04126278. Inclusion in this directory is not an endorsement.