The Efficacy of Superficial Cervical Block Application in Postoperative Analgesia Management in Patients Undergoing Total Laryngectomy and Bilateral Neck Dissection

NACompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

March 10, 2025

Primary Completion Date

July 10, 2025

Study Completion Date

July 12, 2025

Conditions
Laryngeal Neoplasm
Interventions
PROCEDURE

Superficial Cervical Block (SCB) Group

"Patients in this group will receive a bilateral superficial cervical block under ultrasound guidance after anesthesia induction but before the surgical procedure begins.~The block will be performed using 0.1 mL/kg of 0.25% bupivacaine per side, targeting the superficial branches of the cervical plexus.~The primary goal is to assess its efficacy in postoperative pain management and its impact on recovery parameters."

Trial Locations (1)

Unknown

Basaksehir cam and sakura city hospital, Istanbul

All Listed Sponsors
lead

Başakşehir Çam & Sakura City Hospital

OTHER_GOV

NCT06852651 - The Efficacy of Superficial Cervical Block Application in Postoperative Analgesia Management in Patients Undergoing Total Laryngectomy and Bilateral Neck Dissection | Biotech Hunter | Biotech Hunter