Evaluation of the Superficial Cervical Plexus Block in Oncological Throat and Neck Surgery (BCS-ORL)

NCT07110857 NA NOT_YET_RECRUITING

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.

Details

Lead sponsor	Assistance Publique - Hôpitaux de Paris
Phase	NA
Status	NOT_YET_RECRUITING
Enrolment	346
Start date	2025-09
Completion	2027-09

Conditions

• ENT Cancers

Interventions

• Cervical plexus block with 0.2 % Naropeine
• Cervical plexus block with saline placebo

Primary outcomes

• Amount of morphine — The first 24 hours postoperatively
  The analysis metric is the cumulative amount of IV morphine (amount of morphine titrated in SSPI + administered by PCA in mg and mg/kg/day) during the first 24 hours postoperatively.

Countries

France