Comparing two pain relief methods for laparoscopic kidney surgery
Comparison of Erector Spina and Transversus Abdominus Plan Blocks
This study is testing which of two pain relief methods works better for people aged 18 to 65 after laparoscopic kidney surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Kocaeli University Academic / other |
| Locations | 1 site (Kocaeli) |
| Trial ID | NCT05913167 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effectiveness of two analgesic techniques, the erector spina plane block and the transversus abdominis plane block, in reducing postoperative pain for patients undergoing laparoscopic nephrectomy. Patients aged 18 to 65 with an ASA classification of 1 to 3 will be randomly assigned to one of the two groups. Anesthesia will be induced using propofol, fentanyl, and rocuronium, with monitoring of anesthesia depth via bispectral index. The primary outcome measure will be the amount of morphine consumed postoperatively, assessed through a patient-controlled device.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 65 who are scheduled for laparoscopic nephrectomy and have an ASA classification of 1 to 3.
Not a fit: Patients who are younger than 18 or older than 65, those undergoing open nephrectomy, or those with an ASA classification of 4 or 5 may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing laparoscopic nephrectomy.
How similar studies have performed: Previous studies have shown that both erector spina plane block and transversus abdominis plane block can be effective in managing postoperative pain in abdominal surgeries, suggesting potential success for this comparative approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18-65 age * patients undergoing laparoscopic nephrectomy * ASA 1-3 Exclusion Criteria: * \<18- \>65 \< age * patients undergoing open nephrectomy * ASA 4-5
Where this trial is running
Kocaeli
- Kocaeli University — Kocaeli, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Zehra Arslan
- Email: zehraipekarslan@hotmail.com
- Phone: 0090303
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.