Clinical Trial

Analgesic Efficacy of Intertransverse Process Block Versus Erector Spinae Plane Block

Not Yet Recruiting
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Summary
This randomized clinical trial aims to evaluate and compare the analgesic efficacy of the Intertransverse Process Block (ITP) and the Erector Spinae Plane (ESP) block in patients undergoing Robotic Colorectal Surgery. The primary outcome is the Visual Analog Scale (VAS) score within the first 24 hours after surgery. Secondary outcomes include total opioid consumption, requirement for rescue analgesia, block-related and systemic side effects (hematoma, pneumothorax, local anesthetic systemic complications, vascular puncture, and infection), patient and surgeon satisfaction assessed using a Likert scale, and quality of recovery assessed using the QoR-15 questionnaire, and incedence of postoperative nausea and vomiting.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-05-07.
Trial Details
NCT Number NCT07583602
Lead Sponsor Antalya City Hospital
Conditions Robotic Colorectal Surgery, Erector Spine Plane Block, Intertransverse Process Block, Postoperative Pain
Enrollment 50 participants
Start Date 2026-08-30
Primary Completion 2027-12-30 (estimated)
Study Completion 2028-04-30 (estimated)
Updated on ClinicalTrials.gov 2026-05-20