跳至主要内容
临床试验/CTRI/2019/05/018988
CTRI/2019/05/018988招募中不适用

Comparing adductor canal block and multisite infiltration analgesia (intra-articular and peri-articular) in efficient pain control among the cases of unilateral total knee replacement;a prospective randomized controlled trial

AFMC Pune2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年5月13日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
2
主要终点
Time for rescue analgesic, total amount of analgesic required keeping the patient pain free during 48 hours of postoperative period, NRS score

研究概览

简要总结

Most of the previous studies compared the analgesic and other post-op outcomes of various techniques used for early rehabilitation of patients who underwent TKR. Study involving comparison of MIA and ACB is warranted for adoption at Command hospital, Pune and Military hospital, Kirkee. Thus study which will be conducted at entirely proficient and amply loaded tertiary Orthopedic centres will add to the literature explaining the efficiency of the pain management techniques in Total Knee Replacement.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant Blinded

入排标准

年龄范围
0.00 Day(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Age upto 80 yrs, American society of anaesthesiologists grade I to III, Body mass index 18-30 kg/m2.

排除标准

  • Patients with comorbidities (morbid obesity, muscular dystrophy, history of stroke or major neurological deficit, sensory and motor disorders etc.., allergic to LAs and opioids, chronic pain requiring opioid medication, bilateral total knee replacement.

结局指标

主要结局

Time for rescue analgesic, total amount of analgesic required keeping the patient pain free during 48 hours of postoperative period, NRS score

时间窗: 1 yr

次要结局

  • Total amount of analgesic required keeping the patient pain free during 48 hours of postoperative period, NRS score(1 yr)

研究者

发起方
AFMC Pune
申办方类型
Government medical college

研究点 (2)

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