Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair

Recruiting now · Not applicable

Conditions studied: Rotator Cuff Syndrome

In brief

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).

Key facts

Study ID

NCT07093905

Run by

GCS Ramsay Santé pour l'Enseignement et la Recherche

People needed

34

Starts

2026-03-12

Expected to finish

2026-12-01

Last updated by the study team

2026-03-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years;
• Patients with surgically repairable complete or partial rotator cuff tears;
• American Society of Anesthesiologists Class I to III;
• Patient able to understand study information;
• Patient willing to accept study evaluations and follow-up visits;
• Affiliation with a social insurance plan;
• Patient having been informed and having agreed to participate in the study by signing an informed consent form.

You may not qualify if…

• Contraindication to general or locoregional anesthesia;
• Chronic opioid use;
• Patient unable to understand study information (linguistic, psychological, cognitive, etc.);
• Patient unable to answer a self-questionnaire;
• Patient participating in or being excluded from another interventional research study;
• Pregnant or breast-feeding women;
• Protected patient (under legal protection, guardianship or deprived of liberty by judicial or administrative decision).

Where it is running

• Hôpital Privé Clairval — Marseille, France (enrolling)

Full record on ClinicalTrials.gov

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