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To compare between ultrasound guided erector spinae plane block and oblique subcostal transversus plane block pain control in patients after laparoscopic cholecystectomy

Comparative study of the efficacy of ultrasound guided erector spinae plane block and oblique subcostal transversus abdominis plane block for post operative analgesia after laparoscopic cholecystectomy.A randomized clinical trial - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071473
Enrollment
86
Registered
2024-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ultrasound-guided Oblique Subcostal Transversus Abdominis Plane Block: Study Participants will be divided into two groups. Intervention Group B will be given Oblique Subcostal Transvers

Sponsors

SUBU KOBING
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of age 18-70 years with ASA(American Society of Anaesthesiologists)Grade 1 and Grade 2 2.Patients with BMI between 18-30

Exclusion criteria

Exclusion criteria: 1.Patients refusal 2.Patients with known allergy to local anaesthesia 3.Patients with bleeding diathesis,presence of severe kidney,hepatic disease,on anticoagulants,pre-existing cardiovascular disease,chronic opioid consumption,severe or advanced psychiatric illness. 4.Patients with previous upper abdominal surgery,any deformity in spine 5.Patients with infection at the regional block site

Design outcomes

Primary

MeasureTime frame
To evaluate for pain using Numerical Rating Score(NRS)Timepoint: Outcome will be assesed at 0 hour,3rd,6th,9th,12th,18th and 24th hour after the intervention

Secondary

MeasureTime frame
To evaluate total analgesic consumption and time to first rescue analgesia and postoperative nausea and vomitingTimepoint: Outcome will be assesed from the time of intervention and data will be collected at the end of 24 hour

Countries

India

Contacts

Public ContactDr Subu Kobing

RIMS Imphal

drmram6@gmail.com8259055986

Outcome results

None listed

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