Clinical Research Directory
Browse clinical research sites, groups, and studies.
Evaluation of the Superficial Cervical Plexus Block in Oncological Throat and Neck Surgery
Sponsor: Assistance Publique - Hôpitaux de Paris
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
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
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