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临床试验/CTRI/2024/08/071958
CTRI/2024/08/071958尚未招募4 期

COMBINED ADDUCTOR CANAL BLOCK AND IPACK BLOCK VERSUS COMBINED FEMORAL NERVE BLOCK AND SCIATIC NERVE BLOCK FOR POST OPERATIVE ANALGESIA IN TOTAL KNEE ARTHROPLASTY : A PROSPECTIVE RANDOMISED DOUBLE BLIND COMPARATIVE STUDY:

Government Medical College Baroda1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2024年8月15日最近更新:

试验速览

阶段
4 期
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 analgesia using VAS score

研究概览

简要总结

Our goal of study is to compare efficacy of two group of regional blocks For post-operative analgesia in total knee arthroplasty patients.

32 patients will be randomly divided into two groups who are posted for elective total knee arthroplasty.

In one group , ultrasound guided adductor canal block and IPACK block will be given postoperatively .

In second group ,ultrasound guided femoral nerve block and sciatic nerve block (Anterior approach) will be given postoperatively .

Duration of analgesia will be assessed using VAS score till 24hr as a primary outcome .

as a secondary outcome Total number of dose of rescue analgesia given in the 24hr post procedural , Degree of active knee flexion at 20hr and 24hr post procedural using goniometer ,vital parameters at timely interval till 24hr , extent of motor blockage post procedural will be assessed

研究设计

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

入排标准

年龄范围
40.00 Year(s) 至 85.00 Year(s)(—)
性别
All

入选标准

  • Age group- 40-85 yr Either sex ASA –I II III Patient posted for elective Total knee Arthroplasty.
  • Patient able to give verbal and informed consent.
  • Patient able to understand VAS regarding assessment of pain.

排除标准

  • Patient refusal Allergy to local anesthetics.
  • Patient with local site infection Patient with coagulopathy disorder Patient with cognitive and psychiatric illness Patient with peripheral neuropathy and neurological deficit Patient with severe cardiovascular, respiratory, renal and hepatic disease (ASA-IV).

结局指标

主要结局

Duration of analgesia using VAS score

时间窗: till 24 hr

次要结局

  • Number of rescue analgesia required in 24 hrs(Degree of active knee flexion at 20 hr and 24 hr post procedural using goniometer)

研究者

发起方
Government Medical College Baroda
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Rimple Shah

Government Medical College Baroda

研究点 (1)

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