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
Sponsors and collaborators
GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead sponsor
Euraxi Pharma
Collaborator