CTRI/2019/05/019271尚未招募1 期
"Comparison of 0.1% Ropivacaine and 0.0625% Bupivacaine, with fentanyl as an adjuvant for labour analgesia"
G Ranganaayaki1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年5月23日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Pain relief
研究概览
简要总结
With the help of this study, we would like to identify the drug which is safe and long acting with less adverse effects to be used as a labour analgesia. I would like to implicate findings of this study so as to provide adequate analgesia during labour. We would like to compare between 0.1% Ropivacaine and 0.0625% Bupivacaine in releiving labour pain with less or no adverse effects, duration of action of each drug.
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
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- Female
入选标准
- •Parturients requesting epidural analgesia in SMVMCH from May 2019 to September 2020
- •Parturients of ASA physical status 1 and 2 3.Parturients in active labour with cervical dilation of more than 3 cm
- •Full term live fetus without any obstetric complication.
排除标准
- •Height < 150cm 2)BMI >30 3)Age <18 years 4)Anticipated difficult intubation 5)Contraindications for epidural catheter placement 6)Hyper-sensitivity to study drugs.
- •Administration of IV analgesics within 1hr of epidural request.
结局指标
主要结局
Pain relief
时间窗: Visual analog scale score will be recorded every 5 min for first 30 min, then at every 30 min till the end of labor. VAS at the end of the first stage and second stage is also noted.
次要结局
- maternal sedation(sensory blockade)
研究者
研究点 (1)
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