Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

About this trial

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).

Eligibility criteria

Qualifiers

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;

Disqualifiers

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;

Trial design

Treatments tested in this trial

  • arthroscopy of the shoulder rotator cuff

Treatment groups

34 Participants
are divided into 2 treatment groups

Sponsors and collaborators