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Duration of Immobilization After Reverse Total Arthroplasty for Proximal Humerus Fractures

StatusRecruiting
PhaseNot specified
Started
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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.

Record History

  1. Notable Primary completion date: Feb 1, 2024 to Feb 1, 2026 Completion date: Feb 1, 2025 to Feb 1, 2027v2 Show 1 more changeShow less
    • Completion date: Feb 1, 2025 to Feb 1, 2027
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06133920
Lead Sponsor The Cooper Health System
Conditions Proximal Humeral Fracture, Reverse Total Shoulder Arthroplasty
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov