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NCT06729983 · ClinicalTrials.gov registry record · NA
Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty Outcomes
A NA study of Osteoarthritis Shoulder, sponsored by Nickolas Garbis.
- Recruiting
- Registry status
- NA
- Development phase
- 110
- Enrollment target
- 1
- Study location
NCT06729983 is a NA study of Osteoarthritis Shoulder that is actively recruiting participants, run by Nickolas Garbis. The registered enrollment target is 110 participants, below the 356-participant average among 8 other Osteoarthritis Shoulder trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06729983, a NA study of Osteoarthritis Shoulder, is actively recruiting participants, sponsored by Nickolas Garbis.
- RECRUITING
- Registry status
- NA
- Development phase
- 110 participants
- Enrollment target
- 1
- Study location
Study Summary
Some patients may experience persistent pain in the front of their shoulder after reverse shoulder replacement. One of the possible reasons for this is that the surgery causes a change in the alignment of the shoulder joint, which may cause increased tension and compression on one of the biceps tendon called the conjoint tendon. The purpose of this study is to evaluate whether conjoint tendon lengthening, a surgical procedure that involves cutting and lengthening the conjoint tendon in order to reduce tension and compression, is able to prevent or reduce the risk of anterior shoulder pain at one year after surgery.
Conditions Studied
Interventions
- PROCEDURE Prophylactic Conjoint Tendon Lengthening
- PROCEDURE Standard Reverse Shoulder Arthroplasty
Study Locations (1)
Illinois
- Loyola Outpatient Center - Maywood
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2025-03 |
| Est. Completion | 2029-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06729983
The ClinicalTrials.gov registry entry for NCT06729983 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 356-participant average among 8 other Osteoarthritis Shoulder trials with a reported enrollment target (69% lower). The listed sponsor is Nickolas Garbis, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Osteoarthritis Shoulder appearing as the primary indexed condition, and to 2 interventions - of which Prophylactic Conjoint Tendon Lengthening is the first listed.
NCT06729983 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT06729983 about?
NCT06729983 is a clinical study titled "Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty Outcomes". Some patients may experience persistent pain in the front of their shoulder after reverse shoulder replacement. One of the possible reasons for this is that the surgery causes a change in the alignment of the shoulder joint, which may cause increased tension and compression on one of the biceps tend...
What is the current status of trial NCT06729983?
This trial is currently recruiting. It is a NA study. The enrollment target is 110 participants. The study started on 2025-03. Estimated completion is 2029-03.
What conditions does trial NCT06729983 study?
This clinical trial studies the following conditions: Osteoarthritis Shoulder.
What interventions are being tested in trial NCT06729983?
The interventions under investigation include: Prophylactic Conjoint Tendon Lengthening (PROCEDURE), Standard Reverse Shoulder Arthroplasty (PROCEDURE).
Who is sponsoring clinical trial NCT06729983?
This trial is sponsored by Nickolas Garbis, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06729983 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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