Fluoroscopic Endobutton in Clavicle Fractures and AC Dislocations
Condition(s) studied
Investigational drug(s) / intervention(s)
endobutton under fluoroscopic control (Knotless AC TightRope®): endobutton under fluoroscopic contro
Study summary
This study aims to inform clinical decision-making by thoroughly examining the outcomes of different treatment approaches for lateral quarter clavicle fractures and acromioclavicular dislocations. By evaluating the safety and efficacy of Knotless AC TightRope® repair devices and comparing short- and long-term results with other fixation techniques, the investigators hope to contribute to the improvement of treatment protocols for these common shoulder injuries. This research could significantly impact patients' quality of life by enabling optimal recovery and restoration of shoulder function.
Eligibility
Primary outcome measure(s)
- maintaining acromioclavicular reduction — at 6 months
The effectiveness of the endo-button (Knotless Acromioclavicular TightRope®) in maintaining acromioclavicular reduction at 6 months will be assessed through radiological imaging.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Clinique Du Trocadéro | Paris | France | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07664202 on ClinicalTrials.gov ↗ ← All trials in France