NIL

Comparative analgesic efficacy of external oblique intercostal plane block versus subcostal transversus abdominis plane block in adult patients undergoing elective laparoscopic cholecystectomy: A Randomised Controlled Trial . - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/06/111529

Enrollment

Registered

2026-06-01

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-22

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

Conditions

Health Condition 1: - Health Condition 2: K00-K95- Diseases of the digestive system

Interventions

Intervention1: EXTERNAL OBLIQUE INTERCOSTAL PLANE BLOCK .: At the end of laproscopic cholecystectomy surgery groupE will recieve 25 ml of 0.25% bupivacaine (local anesthetic)soln as EOIPB Control Int

Eligibility

Inclusion criteria

Inclusion criteria: Elective laparoscopic cholecystectomy

Exclusion criteria

Exclusion criteria: Coagulopathy Local infection at block site Chronic opioid use Allergy to local anesthetics Conversion to open surgery

Design outcomes

Primary

Measure	Time frame
Total tramadol consumption (mg) in the first 24 hours postoperative periodTimepoint: Total tramadol consumption (mg) in the first 24 hours postoperative period	—

Secondary

Measure	Time frame
Time to first rescue analgesiaTimepoint: nil;NRS pain scores at defined intervalsTimepoint: 0 2 4 6 12 24hrs;Number of rescue analgesic doses requiredTimepoint: nil;Incidence of block-related or opioid-related adverse eventsTimepoint: nil;Patient satisfaction scoreTimepoint: 24hrs	—

Countries

India

Contacts

Public ContactK Venkatesh

Madras Medical College

venkateshkempulraj@gmail.com09445262632

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026

NIL