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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: Recruiting study of Reverse Total Shoulder Arthroplasty and Proximal Humeral Fracture, sponsored by The Cooper Health System.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
the postoperative range of motion (ROM) will be compared between the 2 groups at 2 weeks, 6 weeks, 12 weeks, 6 months, 1 year, and two years
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 |
What NCT06133920 shows while recruiting
NCT06133920 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 236-participant average among 3 other Reverse Total Shoulder Arthroplasty trials with a reported enrollment target (83% lower).
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 a single indexed study location in 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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