Adhesive Capsulitis Clinical Trial
— DOXYOfficial title:
Intra-articular Doxycycline: A Novel Treatment of Adhesive Capsulitis
Verified date | January 2024 |
Source | Vanderbilt University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
We will recruit a total of 40 patients from the Vanderbilt Sports Medicine Clinics who have been diagnosed with adhesive capsulitis and have not undergone any previous treatment. The 40 patients will be randomized, with 20 in the control group of 3 intra-articular injections of 40mg Methylprednisolone spaced every two weeks, and 20 in the experimental group of 3 intra-articular injection of 50mg doxycycline spaced every two weeks. Both groups will begin a standardized physical therapy program within a pain-free range of motion 4 weeks after the initiation of treatment. We will prospectively follow patients for one year, with follow-up at 6 weeks, 12 weeks, 6 months, and 12 months after the initiation of treatment. Outcomes will be measured using the American Shoulder and Elbow Score (ASES) and objective measurements of shoulder range of motion, which will be collected by the treating physician. Both the patients and physicians participating in the study will be blinded.
Status | Completed |
Enrollment | 1 |
Est. completion date | February 8, 2022 |
Est. primary completion date | February 8, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years of age and older, - diagnosis of stage II adhesive capsulitis as determined by clinical examination of the treating physician, and - absence of abnormal findings on X-ray. Exclusion Criteria: - allergy to Doxycycline or Methylprednisolone, - pregnancy, - diagnosis, - Inflammatory arthritis or diabetes, - secondary adhesive capsulitis (history of significant trauma, rotator cuff tear injury, stroke) - evidence of arthritis on x-ray, - current infectious disease, and - any previous treatment for the for adhesive capsulitis of the affected shoulder. |
Country | Name | City | State |
---|---|---|---|
United States | Vanderbilt Medical Center | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University Medical Center | Orthopedic Research and Education Foundation |
United States,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in American Shoulder and Elbow Score (ASES) | The American Shoulder and Elbow Score questionnaire was developed to provide a standardized method for evaluating shoulder function and has been validated in patients with any array of shoulder pathologies. ASES results are in the 0 to 100 range, where 0 indicates a worse shoulder condition and 100 indicates best shoulder condition, so the lower the score, the greater the level of shoulder disability. Transforming the pain and the ADLs domains into the final score relies on the following formulas: Pain = 5 x (10 - Score from question 7) | Baseline and 12 months | |
Primary | Change in Range of Motion(ROM) Measurements | The ROM measurements will include forward flexion, abduction, external rotation at the side and at 90 degrees abduction, and internal rotation at the side and at 90 degrees abduction recorded by the treating physician at follow up visits | Baseline and 12 months | |
Secondary | Number of Medical Co-morbidities | number of medical co-morbidities per participant | Baseline | |
Secondary | Duration of Symptoms | Length of time participants have experienced shoulder symptoms | Baseline | |
Secondary | Changes in Pain | Number of participants with current dominant symptom and/or dominant symptom with disease onset | Baseline | |
Secondary | Pain With Sitting | Number of patients that have pain while sitting or have ever had pain while sitting will be recorded using patient-reported survey and review of the patient's electronic medical record in Epic. | Baseline | |
Secondary | Stiffness | Number of participants with current dominant symptom and/or dominant symptom with disease onset | Baseline |
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