Pain management during laparoscopic gallbladder surgery
Evaluation of Post-Operative Analgesic Efficacy of Bilateral External Oblique Intercostal Plane Block Versus Wound Site Infiltration Control Group in Patients Underwent Laparoscopic Cholecystectomy Surgery
This study tests if a specific pain relief method can help adults aged 18 to 65 feel less pain after laparoscopic gallbladder surgery compared to a different pain relief technique.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06656299 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of the External Oblique Intercostal Plane Block in managing postoperative pain for patients undergoing laparoscopic cholecystectomy. It compares pain scores between patients receiving this block and those receiving infiltration at the trocar entry site. The goal is to enhance patient comfort, reduce complications, and shorten hospital stays by effectively managing pain after surgery. The study involves patients aged 18 to 65 scheduled for elective surgery under general anesthesia.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 65 scheduled for elective laparoscopic cholecystectomy under general anesthesia.
Not a fit: Patients with coagulation disorders, severe organ failure, or those who have had prior abdominal surgeries may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce postoperative pain and improve recovery outcomes for patients undergoing gallbladder surgery.
How similar studies have performed: Previous studies have shown that interfascial plane blocks can effectively manage postoperative pain, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18 to 65 who will be scheduled for an elective laparoscopic cholecystectomy under general anesthesia * ASA (American Society of Anesthesiologists) I-II-III Exclusion Criteria: * presence of coagulation disorder * infection at the injection site of the block * known allergy to local anesthetics * advanced hepatic, heart or renal failure * history of abdominal surgery or trauma * conversion of laparoscopic to open surgery * consumption of any pain killers within the 24 h before the operation * chronic opioid consumption * pregnancy * alcohol or drug abuse * body mass index (BMI) ≥ 35 kg m-2 * Impairment of the patient's cognitive functions (such as Alzheimer's disease, dementia, etc.). * Cholecystectomy cases performed under emergency conditions.
Where this trial is running
Istanbul
- Sancaktepe Şehit Prof. Dr. İlhan Varank Training and Research Hospital — Istanbul, Turkey (Türkiye) (Recruiting)
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.