SPSIPB vs SAPB for Thoracoscopic Surgery

NACompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

August 10, 2024

Primary Completion Date

June 20, 2025

Study Completion Date

June 25, 2025

Conditions
Lung DiseasesLung CancerLung NeoplasmsLung Cancer MetastaticThoracic DiseasesThoracic CancerThoracic Neoplasms
Interventions
DRUG

SPSIPB blcok

A high-frequency linear US probe (11-12 MHz, Vivid Q) will be covered with a sterile sheath, and an 80 mm block needle (Braun 360°) will be used. The procedure will be performed with the patient in the lateral decubitus position. After the scapula is shifted slightly laterally, the US probe is placed sagittal at the upper corner of the spina scapula, and the serratus posterior superior muscle is visualized with the third rib. The in-plane technique will be used. The block needle will be advanced in the craniocaudal direction to enter between the serratus posterior superior and the third rib. The block location will be confirmed by injecting 5 ml of saline between the rib and the muscle. After the block location is confirmed, 30 ml of 0.25% concentration bupivacaine will be used.

DRUG

SAPB block

In the lateral decubitus position, US probe will be placed in a sagittal plane over the midclavicular region of the thoracic cage. Then the 7th rib will be identified in the midaxillary line, followed by the identification of the following muscles overlying the 6th rib: the latissimus dorsi (superficial and posterior), teres major (superior), and serratus muscle (deep and inferior). The needle will be inserted in-plane concerning the ultrasound probe targeting the plane superficial to the serratus anterior muscle. 5 ml saline will be injected for correction. Following confirmation of the correct position of the needle, 30 ml %0.25 bupivacaine will be administered for the block.

DRUG

Postoperative analgesia management

Patients will be administered ibuprofen 400 mgr IV every 8 hours in the postoperative period. A patient-controlled device prepared with 10 mcg/ ml fentanyl will be attached to all patients with a protocol including 10 mcg bolus without infusion dose, 10 min lockout time, and 4-hour limit. If the NRS score is ≥ 4, 0.5 mg kg-1 iv meperidine will be administered as a rescue analgesic. Postoperative patient evaluation will be performed by an anesthesiologist blinded to the procedure.

Trial Locations (1)

34070

Istanbul Medipol University Hospital, Istanbul

All Listed Sponsors
lead

Medipol University

OTHER

NCT06546839 - SPSIPB vs SAPB for Thoracoscopic Surgery | Biotech Hunter | Biotech Hunter