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临床试验/CTRI/2025/07/091450
CTRI/2025/07/091450尚未招募不适用

COMPARISON OF THE DURATION OF POST OPERATIVE ANALGESIA BY ULTRASOUND GUIDED TRANSVERSE ABDOMINIS PLANE BLOCK AND ANTERIOR QUADRATUS LUMBORUM BLOCK IN PATIENTS UNDERGOING INGUINAL HERNIA REPAIR UNDER SUB ARACHNOID BLOCK: DOUBLE BLIND, RANDOMISED CONTROL TRIAL

Dr Pramod1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2025年8月10日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
64
试验地点
1
主要终点
Duration of Post operative Analgesia

研究概览

简要总结

This study is a randomised, double blind, parallel group, single centre trial comparing the duration of post operative analgesia in 2 group, Group A Transverse abdominis plane block and Group B in Quadratus lumborum block under Ultrasound sound guided in 18 yr to 60yr old male patients undergoing Inguinal hernia repair surgery under spinal anaesthesia. Study will be conducted with primary outcome of determining time of 1st dose of rescue analgesia and secondary outcome is assessing NRS score at rest and on cough, objective pain assessment, total doses of additional analgesia received in 24hrs, level of sedation, time of ambulation, level of patient satisfaction

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
18.00 Year(s) 至 60.00 Year(s)(—)
性别
Male

入选标准

  • Patient posted for elective unilateral open inguinal hernioplasty 2) ASA 1 and 2 3) Male gender 4) Age 18-60 years.

排除标准

  • patient not giving consent to participate in study 2) Patient with allergic to medication use 3) Contraindication to spinal anaesthesia.
  • Patient with cardiovascular, neurological, respiratory, renal disorder.

结局指标

主要结局

Duration of Post operative Analgesia

时间窗: Post operative every 15 min in 1st hour and every 30 min till 1st dose of rescue analgesia

次要结局

  • NRS Score at Rest and on coughing till rescue analgesia
  • Objective pain assessment of pain using pin prick test(every 15 min in 1st hour and every 30min till 1st dose of rescue analgesia)
  • Total dose of additional analgesic request(24hrs)
  • Level of sedation using RAMSAY SEDATION SCORE(24hrs)
  • Time of ambulation(24hrs)
  • Level of patient satisfaction using LIKERT SCORE(24hrs)

研究者

发起方
Dr Pramod
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Pramod

Ballari Medical College and Research Centre

研究点 (1)

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