Clinical Trials Directory

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

TypeNameDescription
DRUGBarbotageAdministered as per standard of care
DRUGDexamethasone4 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

Source: ClinicalTrials.gov record NCT04126278. Inclusion in this directory is not an endorsement.