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A clinical trial to study the combined effect of two blocks on post-operative analgesia in patients undergoing laparascopic abdominal surgeries.

A comparative study on the analysis of the combined effect of USG-guided subcostal tap block with rectus sheath block and USG-guided modified BRILMA block with rectus sheath block on post-operative analgesia in patients undergoing laparascopic abdominal surgeries - A prospective randomized control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045500
Enrollment
60
Registered
2022-09-14
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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: Rt subcostal TAP block with B/L rectus sheath block: 39 ml of 0.375% Ropivacaine and 1 ml (500mg) of magnesium sulfate Intervention2: Rt Modified BRILMA block with B/L rectus sheath blo

Sponsors

PRIYANGA A
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA 1 and 2 2. Elective and Emergency laparascopic cholecystectomy 3. BMI less than 30

Exclusion criteria

Exclusion criteria: 1. Open abdominal surgeries 2. Coagulation disorders 3. Local infection at the site of injection 4. Patient refusal

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia between two different blocksTimepoint: 0 mins (At the start of surgery), Every 5 minutes for the first 30 minutes of the surgery, Every 10 minutes for the next 30 minutes of the surgery, Every 15 minutes for the next 30 mins of the surgery, and every hour after arrival at PACU—

Secondary

MeasureTime frame
To compare the incidence of side effects in all groups.Timepoint: 0 mins (At the start of surgery), Every 5 minutes for the first 30 minutes of the surgery, Every 10 minutes for the next 30 minutes of the surgery, Every 15 minutes for the next 30 mins of the surgery, and every hour after arrival at PACU;To compare the intensity of pain in all groupsTimepoint: 0 mins (At the start of surgery), Every 5 minutes for the first 30 minutes of the surgery, Every 10 minutes for the next 30 minutes of the surgery, Every 15 minutes for the next 30 mins of the surgery, and every hour after arrival at PACU;To compare the intra op hemodynamic stability in all the study groups Timepoint: 0 mins (At the start of surgery), Every 5 minutes for the first 30 minutes of the surgery, Every 10 minutes for the next 30 minutes of the surgery, Every 15 minutes for the next 30 mins of the surgery;To compare the total amount of opioid analgesia required in first 24 hours Timepoint: Every hour after the surgery—

Countries

India

Contacts

Public ContactPRIYANGA A

Chettinad Academy of Research and Education

pugalenthi08@yahoo.co.in9489404818

Outcome results

None listed

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