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NCT06133920 · ClinicalTrials.gov registry record
Duration of Immobilization After Reverse Total Arthroplasty for Proximal Humerus Fractures
A clinical trial of Reverse Total Shoulder Arthroplasty and Proximal Humeral Fracture, sponsored by The Cooper Health System.
- Recruiting
- Registry status
- 40
- Enrollment target
- 1
- Study location
NCT06133920 is a study of Reverse Total Shoulder Arthroplasty and Proximal Humeral Fracture that is actively recruiting participants, run by The Cooper Health System. The registered enrollment target is 40 participants, below the 236-participant average among 3 other Reverse Total Shoulder Arthroplasty trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06133920, a study of Reverse Total Shoulder Arthroplasty and Proximal Humeral Fracture, is actively recruiting participants, sponsored by The Cooper Health System.
- RECRUITING
- Registry status
- 40 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- OTHER Early Range of Motion
- OTHER Immobilization
Study Locations (1)
New Jersey
- Cooper University Hospital - Camden
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2021-02-24 |
| Est. Completion | 2027-02-01 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06133920
The ClinicalTrials.gov registry entry for NCT06133920 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 236-participant average among 3 other Reverse Total Shoulder Arthroplasty trials with a reported enrollment target (83% lower). The listed sponsor is The Cooper Health System, which has 39 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Reverse Total Shoulder Arthroplasty appearing as the primary indexed condition, and to 2 interventions - of which Early Range of Motion is the first listed.
NCT06133920 reports 1 study location spanning 1 distinct geographic area - top geographies include New Jersey.
Frequently Asked Questions
What is clinical trial NCT06133920 about?
NCT06133920 is a clinical study titled "Duration of Immobilization After Reverse Total Arthroplasty for Proximal Humerus Fractures". 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 patient...
What is the current status of trial NCT06133920?
This trial is currently recruiting. The enrollment target is 40 participants. The study started on 2021-02-24. Estimated completion is 2027-02-01.
What conditions does trial NCT06133920 study?
This clinical trial studies the following conditions: Reverse Total Shoulder Arthroplasty, Proximal Humeral Fracture.
What interventions are being tested in trial NCT06133920?
The interventions under investigation include: Early Range of Motion (OTHER), Immobilization (OTHER).
Who is sponsoring clinical trial NCT06133920?
This trial is sponsored by The Cooper Health System, which has 39 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06133920 being conducted?
This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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