Clinical Trial

Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair

Study acronym: ALRAGA
Recruiting
View on ClinicalTrials.gov →
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).
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-07-22; most recent amendment 2026-03-13.
Status change: Not Yet Recruiting → Recruiting 2026-03-13
Trial Details
NCT Number NCT07093905
Lead Sponsor GCS Ramsay Santé pour l'Enseignement et la Recherche
Collaborators: Euraxi Pharma
Conditions Rotator Cuff Syndrome
Enrollment 34 participants
Start Date 2026-03-12
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-03-16