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
This trial does not accept healthy volunteersQualifiers
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
Parallel
Treatments tested in this trial
arthroscopy of the shoulder rotator cuff
Procedure/Surgeryminimally invasive surgical procedure in which a camera (arthroscope) is inserted into the shoulder joint
Treatment groups
Trial outcomes
Primary outcomes
length of stay in the Post-Interventional Monitoring Room
The primary endpoint is the length of stay in the Post-Interventional Monitoring Room from discharge from the operating room to an Aldrete score \> 8 leading to discharge from the Post-Interventional Monitoring Room.
Sponsors and contacts
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GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead sponsor
Euraxi Pharma
Collaborator