CTRI/2025/08/093360尚未招募不适用
A Prospective double blind randomised study to compare the effect of intrathecal 0.75 (H) Ropivacaine and 0.5 %(H) Bupivacaine in orthopaedic patients undergoing lower limb surgeries under subarachnoid block
Neetiksha1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年8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
- 40
- 试验地点
- 1
- 主要终点
- Onset and duration of sensory block
研究概览
简要总结
Study to compare the clinical efficacy , safety, hemodynamic effects and complications of hyperbaric fixed intrathecal dose of 0.5 % H bupivacaine and 0.75 % H ropivacaine in patients undergoing lower limb orthopaedic surgies
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patient for orthopaedic lower limb surgery ASAI and II BMI less than 30kg per metre sq Height in between 150 to 180 cm.
排除标准
- •Patient not giving cons ASA III or more Contraindication for SAB SAB converted into GA.
结局指标
主要结局
Onset and duration of sensory block
时间窗: 1 year
Onset and duration of motor block
时间窗: 1 year
Two segments dermatome regression time for sensory blockade
时间窗: 1 year
次要结局
- Time of first requirement of rescue analgesia(Haemodynamic parameters bp and hr)
研究者
Neetiksha
Pt JLNGMC ,chamba, HP
研究点 (1)
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