Clinical Trial

Evaluation of the Superficial Cervical Plexus Block in Oncological Throat and Neck Surgery

Study acronym: BCS-ORL
Not Yet Recruiting
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Summary
This national, prospective, multicenter, randomized study aims to reduce the amount of intravenous morphine (titration + PCA morphine) during the first 24 postoperative hours via a locoregional anesthesia technique in patients undergoing throat and neck cancer surgery.
Trial Details
NCT Number NCT07110857
Lead Sponsor Assistance Publique - Hôpitaux de Paris
Collaborators: Ministry of Health, France
Conditions ENT Cancers
Enrollment 346 participants
Start Date 2025-09
Primary Completion 2027-06 (estimated)
Study Completion 2027-09 (estimated)
Updated on ClinicalTrials.gov 2025-08-08