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RECRUITING Not applicable ClinicalTrials.gov

Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair

Sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche • ClinicalTrials.gov ID: NCT07093905

Registry updated: 2026-09-16
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Description

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).

Interventions

  • arthroscopy of the shoulder rotator cuff (Procedure)
    minimally invasive surgical procedure in which a camera (arthroscope) is inserted into the shoulder joint

Eligibility criteria

Inclusion Criteria: * 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. Exclusion Criteria: * 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).

Conditions

Rotator Cuff Syndrome

Locations

  • Hôpital Privé Clairval — Marseille, France
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record