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Clinical Trials/CTRI/2025/07/090105
CTRI/2025/07/090105
Not yet recruiting
Phase 4

Comparison of postoperative analgesia of laparoscopic-assisted and ultrasound-guided transversus abdominis plane block in patients undergoing laparoscopic nephrectomy.

ABVIMS and RML hospital New Delhi1 site in 1 country70 target enrollmentStarted: August 1, 2025Last updated:

Overview

Phase
Phase 4
Status
Not yet recruiting
Sponsor
ABVIMS and RML hospital New Delhi
Enrollment
70
Locations
1
Primary Endpoint
The difference in VAS score will be observed after laparoscopic nephrectomy using either laparoscopic-assisted or ultrasound-guided transversus abdominis plane block.

Overview

Brief Summary

This study compares the effectiveness of two techniques for performing transversus abdominis plane block in patient undergoing laparoscopic nephrectomy. One group will receive the block using laparoscopic assistance while other group will receive it under ultrasound guidance. The aim is to assess which technique provides better post operative pain relief. The study will evaluate pain score, duration of pain relief, amount of rescue pain medication used, and time taken to perform the block. The finding may help determine if laparoscopic assisted technique is suitable alternative to ultrasound guided method in clinical practice.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • (1) ASA grade 1 and 2 (2) Scheduled for elective laparoscopic Nephrectomy.

Exclusion Criteria

  • 1.History of a local anesthetic allergy 2.History of opioid or alcohol addiction 4.BMI more than 30.

Outcomes

Primary Outcomes

The difference in VAS score will be observed after laparoscopic nephrectomy using either laparoscopic-assisted or ultrasound-guided transversus abdominis plane block.

Time Frame: At 6, 12, and 24 hours postoperatively

Secondary Outcomes

  • The duration of the analgesia in both the group(At 6, 12, and 24 hours postoperatively)
  • The total consumption of rescue analgesia in both the groups(At 6, 12, and 24 hours postoperatively)
  • Time taken for administration of block in both the groups
  • Incidence of post-op nausea and vomiting in both the groups(At 6, 12, and 24 hours postoperatively)

Investigators

Sponsor
ABVIMS and RML hospital New Delhi
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr. Ankita trivedi

ABVIMS and RML hospital New Delhi

Study Sites (1)

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