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NOT YET RECRUITING
NCT07110857
NA

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

Sponsor: Assistance Publique - Hôpitaux de Paris

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

18 Years - 90 Years

Study Type

INTERVENTIONAL

Enrollment

346

Start Date

2025-09

Completion Date

2027-09

Last Updated

2025-08-08

Healthy Volunteers

No

Conditions

Interventions

PROCEDURE

Cervical plexus block with 0.2 % Naropeine

Under ultrasound guidance, a superficial cervical plexus block is performed immediately after induction and before skin incision by injecting 15-25 mL of 0.2 % ropivacaine (Naropeine) uni- or bilateral depending on the surgical incision

PROCEDURE

Cervical plexus block with saline placebo

Under ultrasound guidance, a superficial cervical plexus block is performed immediately after induction and before skin incision by injecting 15-25 mL of 0.9 % saline uni- or bilateral depending on the surgical incision

Locations (7)

CHU de Lille- Hôpital Roger Salengro

Lille, France

Assistance publique - Hôpitaux de Marseille

Marseille, France

AP-HP - Hôpital Lariboisière

Paris, France

Assistance publique - Hôpitaux de Paris

Paris, France

CHU Charles Nicolle

Rouen, France

hôpital Foch

Suresnes, France

Institut Gustave Roussy

Villejuif, France