CTRI/2024/08/072624尚未招募2 期
Comparison of the analgesic efficacy of nalbuphine versus butorphanol as an adjuvant to 0.75 percentage hyperbaric ropivacaine in lower abdominal and lower limb surgeries
DR MRIDULA T V1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年8月28日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Postoperative analgesic duration
研究概览
简要总结
Effective post operative analgesia is an important factor for the early ambulation.This is a type of prospective ,randomised double blinded study in which comparison of analgesic efficacy of nalbuphine and butorphanol as an adjuvant to 0.75% hyperbaric ropivacaine in patient undergoing lower abdominal and lower limb surgeries.Totally there are 2 groups each containing 30 persons and total sample size is 60.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •ASA physical status 1 and 2
- •BMI range of 18.5 to 24.9.
排除标准
- •1.Infection at the site 2.Spinal deformity such as kyphoscoliosis 3.Bleeding disorders 4.Allergic reaction to study drugs 5.Patients on tranquilizers,hypnotics,sedatives and other psychotropic drugs.
结局指标
主要结局
Postoperative analgesic duration
时间窗: Pain assessment 2 hourlies until 12 hours
次要结局
- The onset of sensory and motor blockade
- Duration of sensory blockade(Assessed 2 hourlies until 12 hours of post surgery)
- Duration of motor blockade(Assessed 2 hourlies until 12 hours of post surgery)
研究者
Dr Mridula T V
Karnataka Institute of Medical Sciences
研究点 (1)
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