Comparing pain management techniques for kidney transplant donors
Comparison of Spinal Anesthesia Adjuvant and Quadratus Lumborum Block on the Opioid Requirement and Perioperative Pain of Laparoscopic Kidney Transplant Donor
NA · Indonesia University · NCT06764667
This study is testing two different pain management techniques for kidney transplant donors to see which one helps reduce the need for opioids and manage pain better during and after surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Indonesia University (other) |
| Locations | 1 site (Jakarta Pusat, Jakarta Special Capital Region) |
| Trial ID | NCT06764667 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of spinal anesthesia adjuvant and quadratus lumborum block in reducing opioid requirements and managing perioperative pain in patients undergoing laparoscopic donor nephrectomy. The trial involves patients aged 18-65 with a BMI of 35 or less and ASA physical status 1-2. Participants will receive either spinal anesthesia with an adjuvant or a quadratus lumborum block to assess pain control and opioid usage during and after the procedure.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-65 undergoing laparoscopic donor nephrectomy with a BMI of 35 or less.
Not a fit: Patients with significant cardiovascular issues, recent cerebrovascular disease, or severe renal or liver dysfunction may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for kidney transplant donors, reducing opioid consumption and enhancing recovery.
How similar studies have performed: While similar approaches have been explored, this specific comparison of spinal anesthesia adjuvant and quadratus lumborum block in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18-65 years undergoing laparoscopic donor nephrectomy * Patients with BMI ≤ 35 kg/m2 * Patients with American Society of Anesthesiology (ASA) physical status 1-2 * Patients who are willing to participate in this study Exclusion Criteria: * Cardiovascular disease (uncontrolled stage 2 hypertension, heart failure, arrhytmia) * Recent onset cerebrovascular diseasae of \< 3 months * Infection on spinal site * Coagulopathy * Elevated intracranial pressure * Severe renal or liver dysfunction * Valvular heart disease or atrioventricular block
Where this trial is running
Jakarta Pusat, Jakarta Special Capital Region
- RSUP dr. Cipto Mangunkusumo — Jakarta Pusat, Jakarta Special Capital Region, Indonesia (RECRUITING)
Study contacts
- Study coordinator: Dita Aditianingsih, Prof.
- Email: ditaaditiaa@gmail.com
- Phone: +628151819244
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Laparoscopic Donor Nephrectomy, Perioperative Pain Management, Quadratus lumborum block, Spinal anesthesia adjuvant, Laparoscopic donor nephrectomy, Perioperative pain management