跳至主要内容
临床试验/CTRI/2021/11/038165
CTRI/2021/11/038165尚未招募不适用

Comparison of Levobupivacaine with Ropivacaine in adductor canal block for post operative analgesia in arthroscopic anterior cruciate ligament reconstruction ; a prospective,randomised double blind study

Dr siva rama krishna1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年1月12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
60
试验地点
1
主要终点
to determine duration of analgesia and total rescue analgesic requirement over 24 hrs.

研究概览

简要总结

Local anaesthetics agents are selected for peripheral nerve block for prolonged post operative pain relief with minimum motor blockade. Therefore we wish to conduct this randomized prospective trail to compare effectiveness,duration,and quality of sensory block of levobupivacaine and ropivacaine in appropriate concentrations for post operative analgesia when used for adductor canal block ,performed with ultrasound guidance in patients undergoing arthroscopic anterior cruciate ligament reconstruction surgery.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • elective acl repair surgeries under subarachnoid block and giving consent for post operative adductor canal block.
  • american society of anaesthesiologists physical health status (ASA grade 1 and 2 ).

排除标准

  • ASA 3,4 and 5 allergy to study drugs.
  • pregnant females morbidly obese patients with BMI >35 with height <160cm and >180cm.

结局指标

主要结局

to determine duration of analgesia and total rescue analgesic requirement over 24 hrs.

时间窗: 0,1st,2nd,4th,8th and 24 th hours.

次要结局

  • patient satisfaction score(hemodynamic stability)

研究者

发起方
Dr siva rama krishna
申办方类型
Other [other(self)]

研究点 (1)

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