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A comparative study between erector spinae block and port site local anaesthetic infiltration in laparoscopic cholecystectomy under general anaesthesia

Comparative study between erector spinae block and port site local anaesthetic infiltration in laparoscopic cholecystectomy under general anaesthesia - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110374
Enrollment
176
Registered
2026-05-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: K35-K38- Diseases of appendix Health Condition 2: K20-K31- Diseases of esophagus, stomach and duodenum Health Condition 3: N60-N65- Disorders of breast Health Condition 4: K40-K46- Hernia Health Condition 5: O- Medical and Surgical Health Condition 6: 1- Obstetrics

Interventions

Intervention1: Erector spinae plane block: The study population is divided into 2 groups of 88 patients each- Group E- Landmark guided Bilateral Erector spinae plane block using 20mL of 0.25 percentag

Sponsors

Dr Aarna Garg
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients giving informed written consent for participation in the study. 2. Ageof the patient between 18-65 years of either sex. 3. Patients belonging to ASA class I and II. 4. Patients posted for elective laparoscopic cholecystectomy surgeries under general anaesthesia

Exclusion criteria

Exclusion criteria: 1. Patients who refused consent. 2. Patients with history of chronic pain. 3. Patients with a history of hypersensitivity to the drugs used in study. 4. Patients with coagulation disorders. 5. Patients with morbid obesity (BMI more than 40 kg/m2) 6. Patients with a history of epilepsy or other psychiatric disorders. 7. Pregnant patients. 8. Patients with local infection in the area where ESB would be performed .

Design outcomes

Primary

MeasureTime frame
To compare post operative pain relief in laparoscopic cholecystectomy under general anaesthesia using the Numeric Rating Scale (NRS).Timepoint: Numeric Rating Scale will be assessed at Baseline pre-op, at Baseline post- op, After 6 hours, After 12 hours, After 24 hours

Secondary

MeasureTime frame
To assess Quality of recovery (QoR-15) postoperatively after 24 hours.Timepoint: After 24 hours.

Countries

India

Contacts

Public ContactDr Ajay Kumar Sinha

Government Medical College Haldwani

sinhaak1961@gmail.com9897672301

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026