Clinical Trial

Rectus Abdominis Muscle Parameters and Postoperative Opioid Consumption in Geriatric Patients

Not Yet Recruiting
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Summary
This prospective observational study aims to evaluate the relationship between ultrasound-derived rectus abdominis muscle thickness and thickening fraction and postoperative opioid consumption in geriatric patients undergoing abdominal surgery. Preoperative ultrasonographic measurements will be performed during routine clinical care, and postoperative pain scores and analgesic requirements will be recorded within the first 24 hours. The findings may help improve individualized analgesic strategies by identifying patient-specific predictors of postoperative opioid needs.
Trial Details
NCT Number NCT07545824
Lead Sponsor Istinye University
Conditions Postoperative Pain
Enrollment 62 participants
Start Date 2026-04-25
Primary Completion 2026-10-01 (estimated)
Study Completion 2026-11-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-22