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Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair

RecruitingNAAges 18 Years - anyAllGCS Ramsay Santé pour l'Enseignement et la Recher…
NCT07093905 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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).

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📋 Eligibility rules (as published)
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).
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What it tests

  • arthroscopy of the shoulder rotator cuff
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Where

1 site
Hôpital Privé Clairval
Marseille, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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