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临床试验/CTRI/2017/01/007657
CTRI/2017/01/007657已完成不适用

Adductor canal block for post-operative analgesia after total knee replacement: a randomized controlled trial to study the effect of addition of dexmedetomidine to ropivacaine

Army Hospital Research and Referral Delhi1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2016年1月4日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
The aim of this study is to compare the duration of analgesia of adductor canal block using ropivacaine with and without dexmedetomidine after total knee replacement.

研究概览

简要总结

Total knee replacement is almost alwaysassociated with severe post-operative pain. The current aim of adequateanalgesia and early ambulation is directed at decreased hospital stay andincreased patient satisfaction. Multimodal analgesia such as central andperipheral nerve blocks, NSAIDS, paracetamol, opioids, etc. is most suitablefor this surgery. However, in elderly patients there are concerns about the useof opioids and NSAIDs. The recent success of adductor canal block in providingpost-operative analgesia, along with the prospects of early ambulation hasevoked interest in studying the effects of local anesthetics like ropivacaine,and some adjuvants like dexmedetomidine. Both ropivacaine and dexmedetomidinehave been effectively and safely used in the past in other peripheral nerveblocks.The aim of this study is to compare the durationof analgesia of adductor canal block using ropivacaine with and without dexmedetomidineafter total knee replacement.The secondary outcomes will be the total 24hr opioid consumption, success of early ambulation, level of patient satisfaction,and any adverse effects following the study intervention.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • ASA I-III; BMI 20-30 kg/m2.

排除标准

  • Contraindication to subarachnoid block or allergy to any of the study drugs; Known coagulopathy, local infection at block site; Patients in whom the nerve block could not be performed at per the procedure described in the methodology; Renal dysfunction.

结局指标

主要结局

The aim of this study is to compare the duration of analgesia of adductor canal block using ropivacaine with and without dexmedetomidine after total knee replacement.

时间窗: 15 min, 30 min, 45 min, 60 min, 6 hr, 12 hr, 18 hr, 24 hr

次要结局

  • The secondary outcomes will be the total 24 hr opioid consumption, success of early ambulation, level of patient satisfaction, and any adverse effects following the study intervention.(Medical Research Council Scale as 0-5 at 6, 12, 18 and 24 hr after the block.)

研究者

发起方
Army Hospital Research and Referral Delhi
申办方类型
Research institution and hospital

研究点 (1)

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