CTRI/2024/02/063042尚未招募4 期
A PROSPECTIVE RANDOMISED DOUBLE BLIND CONTROLLED STUDY TO COMPARE INTERATHECAL ROPIVACAINE HEAVY AND BUPIVACAINE HEAVY IN ORTHOPAEDIC SURGERIES.
Pacific medical college and hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年5月3日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- post operative analgesic requirement.
研究概览
简要总结
A study to compare efficacy, onset of block , duration of action ,haemodynamic stability of injection Ropivacaine 0.75% and injection Bupivacaine 0.5% intrathecally in Orthopaedics surgery
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •All patients of age groups between 20 to 60 years of either sex.
- •Patients belong to American Society of Anaesthesiologists (ASA) grade 1 and grade
- •patients posted for lower limb surgeries.
排除标准
- •ASA grade 3 and grade 4 2.congenital anomaly patient 3.Those with bleeding disorders and local sepsis 4.Patients refusal 5.Patients allergic to local anaesthetics.
结局指标
主要结局
post operative analgesic requirement.
时间窗: Duration of analgesia | post operative analgesic requirement. | incidence of shivering till 24hrs after surgery
Duration of analgesia
时间窗: Duration of analgesia | post operative analgesic requirement. | incidence of shivering till 24hrs after surgery
incidence of shivering.
时间窗: Duration of analgesia | post operative analgesic requirement. | incidence of shivering till 24hrs after surgery
次要结局
- duration of analgesia and requirement of rescue analgesia.(24months)
研究者
研究点 (1)
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