Assessing the Impact of Additional Serratus Anterior Block Within 24-Hour on Postoperative Pain After Rhomboid Intercostal Block in VATS Patients

Status: Recruiting
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Design: * Type: Randomized Controlled Trial (RCT) * Participants: 50 patients aged 18 -70 requiring VATS, randomized into two groups: one receiving RIB alone, and the other receiving RIB + SAPB. * Duration: Pain and opioid consumption will be measured within 48 hours post-surgery. * Outcome Measures: Pain levels using the Visual Analog Scale (VAS), opioid usage, and patient satisfaction. Significance: The study addresses the gap in research regarding the combined use of SAPB and RIB in pain control for VATS. It hypothesizes that the combination will lead to better pain relief and reduced opioid dependence compared to RIB alone.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Adults aged 18-70 years.

• Patients undergoing Video-Assisted Thoracoscopic Surgery (VATS).

• Classified as ASA physical status I-III (low to moderate surgical risk).

• Ability to provide informed consent and follow study protocols.

Contact Information
Primary
Mohammed Adel Adwan, MD
maadwan123m@gmail.com
00970594393480
Time Frame
Start Date: 2025-04-01
Estimated Completion Date: 2026-12-01
Participants
Target number of participants: 50
Treatments
Experimental: Arm 1 (RIB Only)
Participants receive a Rhomboid Intercostal Block (RIB) as the sole regional anesthesia technique for postoperative pain management after VATS
Experimental: Arm 2 (RIB + SAPB)
Participants receive both RIB and SAPB within 24 hours postoperatively
Related Therapeutic Areas
Sponsors
Leads: Al-Quds University

This content was sourced from clinicaltrials.gov