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临床试验/CTRI/2021/05/033609
CTRI/2021/05/033609尚未招募不适用

Comparison of Proximal adductor canal block with mid thigh adductor canal block by Ultrasonography defined criteria for post-operative analgesia in total knee replacement surgeries.

Sancheti Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2021年5月25日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
70
试验地点
1
主要终点
Time to first analgesia

研究概览

简要总结

We would like to compare the analgesia efficacy and quadriceps strength between two approaches of saphenous nerve block - first is Proximal adductor canal block and second is Mid-thigh adductor canal block. Time to first analgesia will be noted and total opioid dose requirement during first 24 hours will be noted. quadriceps strength will be assessed 5 hours after block.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
40.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Primary Unilateral Total Knee replacement ASA I and II.

排除标准

  • Revision Total Knee replacement Bilateral TKR Neuropathic joint Symptomatic spine ASA III and IV.

结局指标

主要结局

Time to first analgesia

时间窗: Time to first analgesia | Total opioid requirement in first 24 hours | Quadriceps strength after 5 hours

Total opioid requirement in first 24 hours

时间窗: Time to first analgesia | Total opioid requirement in first 24 hours | Quadriceps strength after 5 hours

Quadriceps strength after 5 hours

时间窗: Time to first analgesia | Total opioid requirement in first 24 hours | Quadriceps strength after 5 hours

次要结局

  • Assessment of quadriceps strength(24 hours)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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