Modified External Oblique Intercostal Plane Block Versus Erector Spinae Plane Block for Open Nephrectomy

Study acronym: EOIPB-ON
StatusRecruiting
PhaseNot applicable
Started

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Record History

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  1. Recruitment opened
    • Eligibility criteria expanded, about 13 words
    • Secondary endpoints: details revised at 1 of 6 entries
    • Site details revised
  2. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
This prospective, randomized, assessor-blinded clinical trial aims to compare the postoperative analgesic efficacy of ultrasound-guided Erector Spinae Plane Block (ESPB) and Modified External Oblique Intercostal Plane Block (EOIPB) in patients undergoing elective open nephrectomy under general anesthesia. Sixty adult patients will be randomized to receive either ESPB or EOIPB before surgical incision. All participants will receive standardized general anesthesia and postoperative multimodal analgesia. Postoperative pain scores, opioid consumption, rescue analgesic requirements, and postoperative nausea and vomiting will be assessed during the first 24 hours after surgery. The study aims to determine whether one fascial plane block technique provides superior postoperative pain control and recovery following open nephrectomy.
Trial Details
NCT Number NCT07726550
Lead Sponsor Namik Kemal University
Conditions
(from sponsor)		 Postoperative Pain, Open Nephrectomy
Related terms Agnosia, Postoperative Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov