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NCT07093905
Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair
Conditions: Rotator Cuff Syndrome
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 34
Sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche
Location: Hôpital Privé Clairval Marseille
Summary
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
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).
Source: ClinicalTrials.gov (NCT07093905). StuddyBuddy aggregates publicly available trial information.