跳至主要内容
临床试验/CTRI/2025/07/091570
CTRI/2025/07/091570尚未招募4 期

Post-operative analgesic efficacy of usg guided ilioinguinal-iliohypogastric nerve block v/s transversus abdominis plane block following caesarean section under subarachnoid block:A Randomised Clinical Trial.

Rajendra Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年8月9日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
To record the time of requirement of first rescue analgesic.

研究概览

简要总结

Effective postoperative analgesia after caesarean section is essential for early recovery, maternal comfort, and newborn care. While spinal (subarachnoid) block is widely used for caesarean delivery, its analgesic effect diminishes over time, often necessitating additional pain control methods.

Ultrasound-guided regional nerve blocks have become valuable tools in multimodal analgesia. Two such techniques—the Transversus Abdominis Plane (TAP) block and the Ilioinguinal-Iliohypogastric (II-IH) nerve block are commonly used to manage somatic pain after lower abdominal surgeries.

The TAP block provides analgesia by anesthetizing the nerves (T6–L1) in the fascial plane between the internal oblique and transversus abdominis muscles, while the II-IH block targets the terminal branches of T12 and L1, supplying the lower abdominal wall. Both blocks have shown effectiveness in reducing postoperative opioid requirements, but their comparative efficacy in caesarean section patients remains uncertain.

This randomized clinical trial aims to compare the postoperative analgesic efficacy of ultrasound-guided II-IH nerve block versus TAP block in women undergoing caesarean section under spinal anesthesia.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
21.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • a)The patient giving written and informed consent for study.
  • b)Patients undergoing C-section will be Primigravida and Multigravida.
  • c)Patients with ASA grade 2.

排除标准

  • a)Patients having weight less than 40kg.
  • b)Patients with deranged coagulation profile.
  • c)Patients having infection at block site.
  • d)Patients having allergy to the study drug.

结局指标

主要结局

To record the time of requirement of first rescue analgesic.

时间窗: Visual Analogue Scale Score | 3hours post-surgery | 6hours post-surgery | 12hours post-surgery | 24hours post-surgery

次要结局

  • a)To record the hemodynamic parameters-systolic blood pressure, diastolic blood pressure,heart rate, MAP.(Baseline)

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Alok Raj

RAJENDRA INSTITUTE OF MEDICAL SCIENCES

研究点 (1)

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