跳至主要内容
临床试验/CTRI/2025/07/090105
CTRI/2025/07/090105
尚未招募
4 期

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 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年8月1日最近更新:

概览

阶段
4 期
状态
尚未招募
发起方
ABVIMS and RML hospital New Delhi
入组人数
70
试验地点
1
主要终点
The difference in VAS score will be observed after laparoscopic nephrectomy using either laparoscopic-assisted or ultrasound-guided transversus abdominis plane block.

概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

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

排除标准

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

结局指标

主要结局

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

时间窗: At 6, 12, and 24 hours postoperatively

次要结局

  • 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)

研究者

发起方
ABVIMS and RML hospital New Delhi
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr. Ankita trivedi

ABVIMS and RML hospital New Delhi

研究点 (1)

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