Adhesive Capsulitis of the Shoulder Clinical Trial
Official title:
Manipulation Under Anesthesia Versus Arthroscopic Capsular Release in the Treatment of Adhesive Capsulitis: A Comparison.
NCT number | NCT01961219 |
Other study ID # | 13-775 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2013 |
Est. completion date | April 25, 2022 |
Verified date | October 2023 |
Source | University of Missouri, Kansas City |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Shoulder pain is one of the most common causes of musculoskeletal disability in the adult population. Adhesive capsulitis is one of a multitude of reasons that can cause shoulder pain and dysfunction. It is a painful and disabling condition that can cause frustration for patients and caregivers due to slow recovery time. It is important to meticulously diagnose the source of the symptoms. Adhesive capsulitis is treatment by non-operative therapies such as physical therapy, exercise, steroids & pain medications. For some patients a quicker return to function is necessary; in th is situation an operative treatment is an option. This study will compare two surgical techniques for adhesive capsulitis. Purpose 1. To directly compare outcomes of patients with adhesive capsulitis who have failed pain management and failed improvement in range of motion after at least 3 months of supervised, regimented conservative treatment and have subsequently been randomized to either closed manipulation under anesthesia or arthroscopic capsular release. 2. To blind both patient and assessing physician/nurse study coordinator to the treatment that was received for the duration of the study. This will reduce the effect of any potential bias on the results as much as possible. 3. To collect outcome data, both subjectively from the patient using proven outcome measures, and objectively from regularly spaced follow up visits with blinded assessors. 4. To collect and comment on data from the two treatment groups regarding duration of post-operative narcotic use, duration of post-operative physical therapy required, post-operative pain levels, and elapsed time until back to work/activity post-operatively.
Status | Terminated |
Enrollment | 13 |
Est. completion date | April 25, 2022 |
Est. primary completion date | April 25, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - patients must be diagnosed as having idiopathic adhesive capsulitis in the 'frozen' or 'thawing' phase of disease and have tried and failed at least 3 months of nonoperative therapy. OR - patient with adhesive capsulitis who presents already in the 'frozen' or 'thawing' phase who demands a quicker return to function and will not try 3 months of nonoperative therapy first. - Age 18 or older Exclusion Criteria: - pregnancy - previously operated shoulder (same side) - other documented source of shoulder pain and stiffness (same side) - rotator cuff tear (same side) - glenohumeral osteoarthritis (same side) - calcific tendonitis (same side) - impingement (same side) - osteonecrosis - neoplasm - cervical radiculopathy - patients who are medically unfit to undergo a general anesthetic - patients who are unable to comply with the post-operative protocol - non-English Speaking patients |
Country | Name | City | State |
---|---|---|---|
United States | Truman Medical Centers | Kansas City | Missouri |
Lead Sponsor | Collaborator |
---|---|
Akin Cil |
United States,
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* Note: There are 26 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | quick Disabilities of the arm, shoulder, and hand (quickDASH) score. | The primary analysis will compare the quickDASH score at the twelve month evaluation between closed manipulation under anesthesia and arthroscopic capsular release using analysis of covariance using the baseline assessment of quickDASH ast he covariate | 12 months post-operatively | |
Secondary | quickDASH score | Secondary analysis will look at all longitudinal evaluation time points of quickDASH using a mixed linear regression model to account for correlations across subjects at multiple time points. | 2 weeks post-operatively | |
Secondary | quickDASH score | Secondary analysis will look at all longitudinal evaluation time points of quickDASH using a mixed linear regression model to account for correlations across subjects at multiple time points. | 4 weeks post-operatively | |
Secondary | quickDASH score | Secondary analysis will look at all longitudinal evaluation time points of quickDASH using a mixed linear regression model to account for correlations across subjects at multiple time points. | 6 weeks post-operatively | |
Secondary | quickDASH score | Secondary analysis will look at all longitudinal evaluation time points of quickDASH using a mixed linear regression model to account for correlations across subjects at multiple time points. | 12 weeks post-operatively | |
Secondary | quickDASH | Secondary analysis will look at all longitudinal evaluation time points of quickDASH using a mixed linear regression model to account for correlations across subjects at multiple time points. | 6 months post-operatively |
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