Pain management using RIFP block in laparoscopic gallbladder surgery
Evaluation of the Effectiveness of Ultrasound-Guided Recto-Intercostal Fascial Plane (RIFP) Block in Postoperative Analgesia Management in Patients Undergoing Laparoscopic Cholecystectomy
This study is testing if a special pain relief technique used during laparoscopic gallbladder surgery can help patients feel less pain and need fewer pain medications afterward.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Istanbul Medipol University Hospital Academic / other |
| Locations | 1 site (Istanbul, Bagcilar) |
| Trial ID | NCT06768593 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness of the Recto-Intercostal Fascial Plane (RIFP) block for managing postoperative pain in patients undergoing laparoscopic cholecystectomy. The RIFP block is performed using ultrasound guidance to inject local anesthetic between the 7th rib and the rectus muscle, targeting specific nerve branches to provide analgesia in the upper abdomen. The study aims to determine if this technique can reduce the need for rescue analgesics and opioid consumption in the first 24 hours post-surgery. By addressing postoperative pain, the trial seeks to improve patient comfort and expedite recovery.
Who should consider this trial
Good fit: Ideal candidates are ASA classification I-II patients scheduled for laparoscopic cholecystectomy under general anesthesia.
Not a fit: Patients with bleeding disorders, those on anticoagulants, or individuals with significant comorbidities such as congestive heart failure or liver/kidney disease may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance pain management and recovery for patients undergoing laparoscopic cholecystectomy.
How similar studies have performed: While RIFP blocks have shown effectiveness in other surgical contexts, this specific application in laparoscopic cholecystectomy is novel and has not been previously studied.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * American Society of Anesthesiologists (ASA) classification I-II patients * Laparoscopic cholecystectomy operation under general anesthesia Exclusion Criteria: patients with * with a history of bleeding diathesis * v receiving anticoagulant treatment, * with allergies or sensitivity to drugs used, * with an infection on the puncture site * with a history of alcohol or drug addiction, * with congestive heart failure * with liver or kidney disease * who do not accept the procedure or participate in the study
Where this trial is running
Istanbul, Bagcilar
- Istanbul Medipol University Mega Hospital Complex — Istanbul, Bagcilar, Turkey (Recruiting)
Study contacts
- Study coordinator: AYSE INCE, Assist Prof
- Email: drayseince@gmail.com
- Phone: +90 5366774988
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.