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Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair

Study acronym: ALRAGA
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Dec 2026 → Apr 30, 2027
See other at-risk trials from GCS Ramsay Santé pour l'Enseignement et la Recherche

Record History

See every version on ClinicalTrials.gov ↗

  1. Lead sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche to GCS Ramsay Santé pour l'Enseignement et la Recherche
    • Primary and study completion pushed from Dec 2026 to Apr 30, 2027
    • Eligibility criteria expanded, about 14 words
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jan 2026 to Mar 12, 2026
    • Site details revised
    v3
  3. Start date: Aug 2025 to Jan 2026
    • Primary and study completion dates: Sep 2026 to Dec 2026
    v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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).
Trial Details
NCT Number NCT07093905
Lead Sponsor GCS Ramsay Santé pour l'Enseignement et la Recherche
Collaborators: Euraxi Pharma
Conditions
(from sponsor)		 Rotator Cuff Syndrome
Enrollment 34 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov