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Pain relief for laparoscopic gallbladder removal

A Randomized Controlled trial On The Efficacy of Pre emptive Laparoscopy Assisted Subcostal Transversus Abdominis Plane Block Compared with that of Port Site Infiltration in providing Post Operative Analgesia following Laparoscopic Cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054243
Enrollment
60
Registered
2023-06-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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: Group A: under direct laparoscopic vision, and when the needleâ??s tip is positioned at the fascial space between the internal oblique and the transversus abdominis muscle, 30 cc of dil

Sponsors

SRM Institute of Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients with cholelithiasis admitted under the General Surgery department in SRM Medical College Hospital and Research Centre fulfilling the following criteria: ASA I, II Age-18-80 Consent to participate in the study

Exclusion criteria

Exclusion criteria: â?? Patients allergic to the local anaesthetic â?? Patients with previous history of coagulopathies/ cardiac diseases â?? Patients with skin diseases of anterior abdominal wall â?? Patients undergoing emergency surgery â?? Patients contraindicated for General Anaesthesia â?? Patients cleared for anaesthesia under ASA III/IV â?? Patients who underwent previous abdominal surgeries â?? Patients unwilling to participate in study

Design outcomes

Primary

MeasureTime frame
Post operatively, VAS (Visual Analogue Score) will be assessed at 1st hour, 4th hour, 8th hour, 16th hour and 24 hours following surgery.Timepoint: Post operatively, VAS (Visual Analogue Score) will be assessed at 1st hour, 4th hour, 8th hour, 16th hour and 24 hours following surgery.

Secondary

MeasureTime frame
complications,HemodynamicsTimepoint: at omin, 1omin, 20 min 30 min every 30min for 2 hrs & hourly for 24 hrs

Countries

India

Contacts

Public ContactDr Athira Gopinathan

SRM Institute Of Science and Technology

balamurr@srmist.edu.in9841434506

Outcome results

None listed

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