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Clinical Trials in Turkey / NCT07661693
Starting soon Not applicable

ESP vs Subcostal TAP Block for Analgesia After Laparoscopic Cholecystectomy

NCT07661693 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2027-06-15
Last updated
2026-06-22

Condition(s) studied

Cholelithiasis, Postoperative Pain, Laparoscopic Cholecystectomy

Investigational drug(s) / intervention(s)

Erector Spinae Plane BlockSubcostal Transversus Abdominis Plane Block

Erector Spinae Plane Block: Ultrasound-guided bilateral erector spinae plane block will be performed after induction of general anesthesia. The block will be administered at the appropriate thoracic vertebral level using a standardized volume and concentration of local anesthetic deposited in the fascial plane deep to the erector spinae muscle. The procedure will be performed by experienced anesthesiologists under sterile conditions.

Subcostal Transversus Abdominis Plane Block: Ultrasound-guided bilateral subcostal transversus abdominis plane block will be performed after induction of general anesthesia. A standardized volume and concentration of local anesthetic will be injected into the fascial plane between the rectus abdominis and transversus abdominis muscles along the subcostal margin. The procedure will be performed by experienced anesthesiologists under sterile conditions.

Study summary

This prospective, randomized, double-blind study compares the analgesic efficacy of ultrasound-guided erector spinae plane (ESP) block and subcostal transversus abdominis plane (TAP) block in patients undergoing laparoscopic cholecystectomy. The primary outcome is 24-hour postoperative opioid consumption. Secondary outcomes include postoperative pain scores, time to first analgesic request, shoulder pain, postoperative nausea and vomiting, and block-related complications.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: Adults aged 18 years and older Scheduled for elective laparoscopic cholecystectomy under general anesthesia American Society of Anesthesiologists (ASA) physical status I-III Ability to understand the study protocol and provide written informed consent - Exclusion Criteria:Refusal to participate Known allergy or contraindication to local anesthetic agents Coagulopathy or anticoagulant therapy contraindicating regional anesthesia Infection at the planned injection site Body mass index (BMI) \> 35 kg/m² Chronic opioid use or opioid dependence Chronic pain syndromes requiring regular analgesic treatment Severe hepatic, renal, or cardiac dysfunction Pregnancy or breastfeeding Inability to communicate or assess pain using the Numerical Rating Scale (NRS) \-

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gaziantep City Hospital Şahinbey Gaziantep

More Gaziantep City Hospital trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07661693 on ClinicalTrials.gov ↗ ← All trials in Turkey