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Comparison of three methods of pain relief in patients undergoing gall bladder surgery

A RANDOMIZED CONTROLLED TRIAL COMPARING THE EFFICACY OF USG TAP BLOCK, PORT SITE INFILTRATION AND INTRAPERITONEAL INSTILLATION FOR POST- OPERATIVE ANALGESIA AFTER LAPAROSCOPIC CHOLECYSTECTOMY - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/03/003493
Enrollment
150
Registered
2013-03-18
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: null- patients scheduled to undergo laparoscopic cholecystectomy

Interventions

Intervention1: Ultrasound guided transversus abdominis plane block(USG TAP) 0.375 ropivacaine: To compare USG TAP,intraperitoneal instillation,port site infiltration for post operative pain relief wit

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • ASA physical status I-II • Age 18-65 yrs • Body weight 50-75 kg of either sex ( BMI - >18.5 to

Exclusion criteria

Exclusion criteria: • History of relevant drug allergy • Age 18yrs or 65yrs • History of psychiatric illness , substance abuse , or medical therapies resulting in tolerance to opioids • Acute cholecystitis or pancreatitis • Severe cardiovascular , respiratory ,metabolic or neurological disease • Surgery requiring postoperative intra-abdominal drainage • Pregnancy

Design outcomes

Primary

MeasureTime frame
To compare and evaluate post operative pain scores after administration of US guided TAP block, port site infiltration and intraperitoneal instillation with ropivacaine in laparoscopic cholecystectomy.Timepoint: To compare and evaluate post operative pain scores after administration of US guided TAP block, port site infiltration and intraperitoneal instillation with ropivacaine in laparoscopic cholecystectomy in the immediate post operative period and then at 10 min, 30 min, 60 min, 4 hours, 8 hrs, 12 hrs and 24 hrs.

Secondary

MeasureTime frame
1.To compare and evaluate post operative nausea and vomiting scores. 2. To calculate the total amount of rescue analgesic used in all the patients. 3. To note any side effect due to the technique or the drug used for the post operative pain relief. Timepoint: Post operative period upto 24 hrs

Countries

India

Contacts

Public ContactDr Richa Saroa

Government medical college and Hospital, Chandigarh

richajayant@rediffmail.com919646121513

Outcome results

None listed

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