Comparison usefulness of Modified Brilma Block using Ultrasound with Block given below the ribs in the stomach in providing Pain Relief after Laproscopy guided Gall Bladder Removal Surgeries

Comparison of Ultrasound-guided Modified Brilma Block with Subcostal Tranversus Abdominis Plane Block for Postoperative Analgesia in Laparoscopic Cholecystectomy â?? A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/02/023457

Enrollment

Registered

2020-02-20

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: G978- Other intraoperative and postprocedural complications and disorders of nervous system

Interventions

Intervention1: Ultrasound Guided Modified Brilma Block: Ultrasound Guided Modified Brilma block for Postoperative analgesia in patients undergoing Laproscopic Cholecystectomy Control Intervention1: Ul

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with ASA Physical Status I and II posted for Laproscopic Cholecystectomy 2. Weighing between 50-100kg 3. Age group of 18-60 years

Exclusion criteria

Exclusion criteria: 1. All patients with ASA Physical Status III and above 2. Patients who refuse to participate in the study 3.Patients who are allergic to amide local anaesthetics 4.Patients who are pregnant 5.Patients with chronic cardiac , renal or hepatic condition 6. Patients with coagulation abnormalities

Design outcomes

Primary

Measure	Time frame
Duration fo Postoperative AnalgesiaTimepoint: Duration fo Postoperative Analgesia	—

Secondary

Measure	Time frame
1.Consumption of Morphine in PCA Pump 2. Intraoperative consumption of opioids 3. ComplicationsTimepoint: 24 hours	—

Countries

India

Contacts

Public ContactKarthika Urkavalan

SRM Medical College Hospital and Research Center

drvenkat94@gmail.com9894581455

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 15, 2026