Trials / Recruiting
RecruitingNCT07093905
Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair
Prospective, Randomized Study Comparing General Anesthesia Combined With Locoregional Anesthesia to Locoregional Anesthesia Alone for Arthroscopic Rotator Cuff Repair.
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 34 (estimated)
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to to compare the post-anesthetic recovery time to awake consciousness and hemodynamic and ventilatory capacities for discharge from the Post-Interventional Monitoring Room in patients admitted for shoulder rotator cuff arthroscopy (using local anesthesia versus general anesthesia + local anesthesia).
Detailed description
This is a prospective, comparative, randomized, open-label, multicenter study comparing two analgesic strategies used in outpatient, routine surgery. The study population is composed of adult patients with complete or partial rotator cuff tears requiring reconstructive surgery under anesthesia at Hôpital Privé Clairval or Clinique Monticelli-Vélodrome. Patients will be seen three times: at inclusion (during the preoperative consultation with the anesthetist), on the day of surgery (hospitalization), and at the follow-up visit (during the postoperative consultation with the surgeon). They will also be contacted by telephone on D1, D3 and D15 to optimize their follow-up. The duration of each patient's participation is approximately one month.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | arthroscopy of the shoulder rotator cuff | minimally invasive surgical procedure in which a camera (arthroscope) is inserted into the shoulder joint |
Timeline
- Start date
- 2026-03-12
- Primary completion
- 2026-12-01
- Completion
- 2026-12-01
- First posted
- 2025-07-30
- Last updated
- 2026-03-16
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT07093905. Inclusion in this directory is not an endorsement.