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
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.)
