CTRI/2024/05/068208招募中4 期
Efficacy of Fentanyl and Butorphanol as adjuvant with 0.5% Hyperbaric Levobupivacaine in caesarean section A Randomised Controlled Double Blind Study
Pithani Vamsee Priya1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2024年6月15日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 160
- 试验地点
- 1
- 主要终点
- Sensory block(In seconds)
研究概览
简要总结
Since levobupivacaine is being used as a safer alternative to bupivacaine plain in spinal anesthesia for caesarean section,there are very limited studies comparing efficacy of butorphanol and fentanyl as adjuvants to levobupivacaine in caesarean section and hence this study is taken up to assess the changes in efficacy of both these opioid drugs when used as adjuvant with levobupivacaine
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- Female
入选标准
- •Pregnant females posted for LSCS under spinal anaesthesia ASA-II.
排除标准
- •Patients not willing to be part of study Contraindications of subarachnoid block Allergy to local anaesthesia Twin pregnancies Polyhydramnios.
结局指标
主要结局
Sensory block(In seconds)
时间窗: The onset of sensory block will be assessed with a pinprick test (using a blunt 25-gauge needle along the mid-clavicular line bilaterally) every 15 seconds from time of subarachnoid block until T6 level achieved.
次要结局
- 1.2 segment regression (in minutes)(2.Duration of sensory block(in minutes))
研究者
Dr PITHANI VAMSEE PRIYA
Kalinga Institute Of Medical Sciences
研究点 (1)
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