Clinical Trial

Duration of Immobilization After Reverse Total Arthroplasty for Proximal Humerus Fractures

Recruiting
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Record status
This record was last updated August 20, 2024 (before its estimated February 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
The purpose of this study is to evaluate compare postoperative range of motion in patients who are given a sling for comfort only and allowed to start early active range of motion compared to patients who are placed in a sling for 4 weeks with passive range of motion only. Once enrolled, the patients will be randomized through computer randomization then placed in paper packets into either the immobilization group or the early range of motion group.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2023-11-14.
Trial Details
NCT Number NCT06133920
Lead Sponsor The Cooper Health System
Conditions Proximal Humeral Fracture, Reverse Total Shoulder Arthroplasty
Enrollment 40 participants
Start Date 2021-02-24
Primary Completion 2026-02-01 (estimated)
Study Completion 2027-02-01 (estimated)
Updated on ClinicalTrials.gov 2024-08-20