Clinical Trials Directory

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

TypeNameDescription
PROCEDUREarthroscopy of the shoulder rotator cuffminimally 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.