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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • arthroscopy of the shoulder rotator cuff

    Procedure/Surgery

    minimally invasive surgical procedure in which a camera (arthroscope) is inserted into the shoulder joint

Treatment groups

34 Participants
are divided into 2 treatment groups
Group A: Locoregional anesthesiaExperimental treatment 1 intervention
Group B: Locoregional anesthesia + general anesthesiaActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
Day 0

Secondary outcomes

Other outcomes

Sponsors and contacts

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