CTRI/2022/06/043360招募中4 期
A comparative study of spinal anaesthesia with hyperbaric Ropivacaine 0.75% and hyperbaric Bupivacaine 0.5% in hypertensive patients undergoing lower abdominal surgery and lower limb surgery
IGIMS1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2022年6月21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
- 80
- 试验地点
- 1
- 主要终点
- Heart rate, Blood pressure, mean arterial pressure recordings
研究概览
简要总结
we aimed to study the effectiveness of Ropivacine 0.75% and Bupivacaine 0.5% in patients with controlled hypertension undergoing surgery under spinal anaesthesia . The aim to study and evaluate the onset and duration of motor and sensory blockade of Ropivacaine 0.75% and Bupivacaine 0.5% and also the hemodynamic stability of patients and post operative analgesia.
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
- 25.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •hypertensive patients, controlled blood pressure both male and female of age group 25- 70 years undergoing surgery under spinal anaesthesia .
排除标准
- •1.Patient refusal for procedure.
- •2.ASA grade > III, IV 3.Emergency Surgery 4.Immunocompromised patients 5.All contraindications for Regional anaesthesia
- •Those with bleeding disorders and local sepsis.
- •Those on anticoagulant and antiplatelet agent.
- •Those allergic to amide anaesthetics.
结局指标
主要结局
Heart rate, Blood pressure, mean arterial pressure recordings
时间窗: 1min, 3min, 5min, 10min,15min,30min, 45min, 60 min intraoperative and postoperative period.
次要结局
- modified bromage score for motor block assessment, global patient satisfaction scale, and patient comfort score(in the post operative period upto 3-4 hrs)
研究者
研究点 (1)
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