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Clinical Trials in Turkey / NCT07653490
Recruiting Not applicable

Erector Spinae Plane Block and Low-Flow Anaesthesia in Laparoscopic Cholecystectomy

NCT07653490 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-18
Last updated
2026-06-23

Condition(s) studied

Postoperative PainLaparoscopic Cholecystectomy

Investigational drug(s) / intervention(s)

Erector Spinae Plane BlockLow Fresh Gas Flow (0.5 L/min)Standard Fresh Gas Flow (3 L/min)Bupivacaine →Sevoflurane →

Erector Spinae Plane Block: Bilateral ultrasound-guided erector spinae plane block (ESPB) will be performed preoperatively at the T7-T8 level

Low Fresh Gas Flow (0.5 L/min): Low-flow anaesthesia will be maintained with sevoflurane using a fresh gas flow rate of 0.5 L/min after the initial high-flow phase following induction of general anaesthesia.

Standard Fresh Gas Flow (3 L/min): Standard-flow anaesthesia will be maintained with sevoflurane using a fresh gas flow rate of 3 L/min throughout the maintenance phase of general anaesthesia.

Bupivacaine: Bupivacaine 0.25% will be administered bilaterally during ultrasound-guided erector spinae plane block at the T7-T8 level, with 20 mL injected on each side approximately 30 minutes before surgery.

Sevoflurane: Sevoflurane will be used as the inhalational anaesthetic agent for maintenance of general anaesthesia during elective laparoscopic cholecystectomy. The fresh gas flow rate during maintenance will be determined according to study group allocation.

Study summary

This prospective randomized controlled study aims to evaluate the effects of preoperative ultrasound-guided erector spinae plane (ESP) block combined with low-flow anaesthesia on postoperative quality of recovery and opioid consumption in patients undergoing elective laparoscopic cholecystectomy. The study will compare postoperative recovery quality, pain scores, analgesic requirements, and perioperative outcomes between patients receiving ESP block with low-flow anaesthesia and those receiving standard anaesthetic management.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18-65 years * ASA physical status I-II * Body mass index (BMI) \<35 kg/m² * Scheduled for elective laparoscopic cholecystectomy * Ability to provide written informed consent Exclusion Criteria: * Coagulopathy or bleeding disorders * Allergy to local anaesthetic agents * Infection at the block application site * Neurological or psychiatric disorders * Communication difficulties * Chronic opioid or analgesic use * Reoperation cases * Acute cholecystitis * Conversion to open surgery * Inadequate dermatomal block after ESPB * Severe intraoperative hemodynamic instability * Intraoperative blood loss ≥250 mL * Development of allergic reactions or major complications during follow-up

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Taksim Training and Research Hospital Istanbul Turkey (Türkiye) Recruiting

More Taksim Egitim ve Arastirma Hastanesi trials in Turkey

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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 NCT07653490 on ClinicalTrials.gov ↗ ← All trials in Turkey