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Effect of ESP Block on Stress Response During Laparoscopic Gallbladder Surgery: A Randomized Trial

Effect of Ultrasound Guided Erector Spinae Plane Block in Attenuation of Stress Response to Pneumoperitoneum in Laparoscopic Cholecystectomy- A Randomized Clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087210
Enrollment
60
Registered
2025-05-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K80-K87- Disorders of gallbladder, biliary tract and pancreas Health Condition 2: K808- Other cholelithiasis

Interventions

Intervention1: Erector Spinae Plane Block: Patients will receive ESPB with 20ml 0.25% ropivacaine bilaterally before surgery after induction of anaesthesia. Control Intervention1: Erector Spinae Plane

Sponsors

Prithibiraj Ahanthem
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of American Society of Anaesthesiologists (ASA) physical grade I or II.

Exclusion criteria

Exclusion criteria: 1. Patient with hypertension 2. Diabetes mellitus with neuropathy 3. Deranged liver and renal function 4. Conversion to open cholecystectomy 5. Patients with known allergy to local anaesthetic drugs 6. Infection at injection site 7. Bleeding disorders

Design outcomes

Primary

MeasureTime frame
To assess the effect of ultrasound guided erector spinae plane block, in attenuation of stress response to pneumoperitoneum and intraoperative opioid consumption in patient undergoing laparoscopic cholecystectomyTimepoint: Total amount of fentanyl consumed during intraoperatively and the response of haemodynamic parameters (Heart Rate, Mean Arterial Pressure) during time of port insertion and at 5 min, 10 min, after pneumoperitoneum stretch, will be recorded.Outcome will be assessed starting from the point of administration of study drugs till 60 minutes post pneumoperitoneum. Data will then be assessed at the end of one year.

Secondary

MeasureTime frame
To evaluate adverse reactions such as hypotension, bradycardia and local anaesthetic toxicity.Timepoint: Outcome will be assessed starting from the point of administration of study drugs till 30 minutes post extubation. Data will then be assessed at the end of one year.

Countries

India

Contacts

Public ContactDr N Ratan Singh

Regional Institute of Medical Sciences, Imphal

drnratansingh@gmail.com919436027270

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026