Hormone Replacement Therapy added to standard care for frozen shoulder in peri- or postmenopausal women
Official title: Hormone Replacement Therapy as an Adjunct Treatment for Adhesive Capsulitis of the Shoulder (Frozen Shoulder) in Peri- and Postmenopausal Women
Run by University of California, San Francisco · NCT07278323 · Data updated 2026-11-12
This study tests whether adding hormone replacement therapy to standard treatment helps reduce pain and stiffness from frozen shoulder in peri- or postmenopausal women.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 40 Years and up |
| Sex | Women only |
| Enrollment | 60 (estimated) |
| Sponsor | University of California, San Francisco Academic / other |
| Locations | 1 site (San Francisco, California) |
| Status | Recruiting |
| Started | January 15, 2026 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | June 8, 2026 |
| Trial ID | NCT07278323 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women who are peri- or postmenopausal with a diagnosis of adhesive capsulitis seeking standard care for frozen shoulder.
✕Probably not a fit
Participants who do not respond to hormonal treatment or who experience adverse effects may not derive additional benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, phase 4 trial compares hormone replacement therapy plus standard care to standard care alone for adhesive capsulitis in peri- or postmenopausal women. All participants receive physical therapy and a joint steroid injection; the experimental group also uses an HRT patch and daily pill. Outcomes include patient-reported shoulder function, range of motion, and a motion-analysis assessment over six months. The study aims to determine if hormonal support can improve pain, mobility, and daily function beyond standard care. Sixty eligible women will be enrolled and followed prospectively at UCSF.
Why it matters
Potential benefit: If successful, participants receiving HRT may experience greater improvements in shoulder pain and motion compared with standard care alone.
How similar studies have gone: Previous research has explored hormonal influences on shoulder pathology, but this specific HRT adjunct for frozen shoulder is novel and its efficacy remains to be demonstrated.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of adhesive capsulitis of the shoulder Exclusion Criteria: * History of hormone sensitive cancer * Bilateral adhesive capsulitis of the shoulder * Currently using hormonal treatments including contraceptives
Where it's running
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UCSF Orthopaedic Institute
San Francisco, California, United States Recruiting
Study contacts
- Principal investigator: Stephanie E Wong, MD — University of California, San Francisco
- Study coordinator: Alexa J Chandler, PhD
- Email: alexa.chandler@ucsf.edu
- Phone: (415) 353-2808
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.