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Not yet recruiting NCT07545824

Rectus Abdominis Muscle Parameters and Postoperative Opioid Consumption in Geriatric Patients

Conditions: Postoperative Pain

Sponsor: Istinye University

trial.available_in: БГ
Overview
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.
Who can participate
Inclusion Criteria: * Age ≥65 years * Scheduled for elective midline abdominal surgery * ASA physical status I-III * Planned to receive bilateral ultrasound-guided rectus sheath block as part of routine clinical practice * Provided written informed consent Exclusion Criteria: * Known allergy or hypersensitivity to local anesthetics * Infection or skin lesion at the injection site * Systemic infection or sepsis * Coagulopathy (INR \>1.5 or platelet count \<100,000/mm³) * Use of therapeutic anticoagulation not safely managed perioperatively * History of previous midline laparotomy * History of abdominal mesh implantation or abdominal wall reconstruction * Significant abdominal wall pathology (e.g., large hernia) affecting anatomy * Neuromuscular disease (e.g., myasthenia gravis, ALS, muscular dystrophy) * Inability to perform required maneuver for dynamic ultrasound measurement * Moderate to severe cognitive impairment or poor cooperation * Body mass index (BMI) \>40 kg/m² * Cachexia or severe malnutrition * Chronic opioid use (≥3 months) * Chronic pain syndromes requiring regular analgesic use * Alcohol or substance abuse * Emergency surgery * Use of additional regional anesthesia techniques (e.g., epidural, TAP block) * Inadequate ultrasound visualization of the target anatomical plane
Interventions
Ultrasound-Guided Rectus Sheath Block
OTHER
Locations 1
Turkey (1)
Istinye Üniversity
Istanbul , Merkez Mahallesi
Technical details
Status
Not yet recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
65 Years
Healthy volunteers
No
Start date
25.04.2026
Completion date
01.11.2026
Registry ID
NCT07545824
Source
clinicaltrials.gov
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