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临床试验/CTRI/2025/09/095249
CTRI/2025/09/095249尚未招募不适用

A Comparative Study of Epidural 0.5 percent Bupivacaine With 30 micrograms [mcg]Buprenorphine Versus Epidural 0.5 percent Bupivacaine With 60 micrograms [mcg]Buprenorphine For Lower Limb Orthopaedic Surgeries-Randomised Control Study

Government medical college,Ananthapuramu1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年9月30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
80
试验地点
1
主要终点
Outcomes were assessed and compared in terms of time taken for the onset of sensory blockade ,motor blockade,duration of motor blockade , duration of sensory analgesia and hemodynamic changes.

研究概览

简要总结

This study is an attempt to compare 0.5% bupivacaine with 30  mcg buprenorphine and 0.5% bupivacaine with 60 mcg buprenorphine for epidural anaesthesia in patients scheduled for lower limb orthopaedic surgeries which alleviates severe post operative pain and decreases the need of iv opioids in post operative period.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients posted for elective lower limb orthopaedic surgeries.
  • Patients in ASA grade 1,2,3 .

排除标准

  • Patients with contraindications for epidural anaesthesia.
  • Uncooperative patients /patient refusal.
  • Pregnant Patients with Spinal deformities Patients with hypersensitivity to the study drug.
  • Coagulation defect /Anticoagulant therapy Sepsis.

结局指标

主要结局

Outcomes were assessed and compared in terms of time taken for the onset of sensory blockade ,motor blockade,duration of motor blockade , duration of sensory analgesia and hemodynamic changes.

时间窗: 2 weeks, 4 weeks and 8 weeks

次要结局

  • Side effects recorded(and compared)

研究者

发起方
Government medical college,Ananthapuramu
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Yuvakeerthana R

Government medical college,Ananthapuramu

研究点 (1)

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