Rectus Abdominis Muscle Parameters and Postoperative Opioid Consumption in Geriatric Patients (NCT07545824) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Rectus Abdominis Muscle Parameters and Postoperative Opioid Consumption in Geriatric Patients
Turkey (Türkiye)62 participantsStarted 2026-04-25
Plain-language 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.
Who can participate
Age range
65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.