CTRI/2019/02/017789已完成不适用
Effect of intrathecal dexmedetomidine as an adjuvant to low‑ dose bupivacaine in patients undergoing transurethral resection of prostate - A prospective randomised - double blind study
Department of anaesthesiology Jln Medical College ajmer1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年2月25日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Duration of analgesia
研究概览
简要总结
To study the effects of intrathecal dexmedetomidine as an adjuvant to low dose bupivacaine in patients undergoing transurethral resection of prostate with respect to: PRIMARY OBJECTIVE: 1. Duration of analgesia SECONDARY OBJECTIVES: 1. Block characteristics (onset and duration of sensory and motor block ). 2. First rescue analgesic requirement. 3. Total rescue analgesic requirement in 24 hour. 4. Haemodynamic changes. 5. Side effects, if any.
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
- 50.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- Male
入选标准
- •1.Male patients between 50 to 70 years of age.
- •2.ASA physical status 1,2 and 3.
排除标准
- •ASA physical status 4,5 &
- •Patients refusal.
- •Patients with peripheral sensorineural deficit.
- •Patients is sensitive or allergic to study medications.
结局指标
主要结局
Duration of analgesia
时间窗: Duration of study is around 1 year
次要结局
- 1. ASA physical status 4,5 and 6. 2. Patients refusal. 3. Patients with peripheral sensorineural deficit. 4. Patients is sensitive or allergic to study medications. 5. Patients on anticoagulants. 6. Infection at the site of of lumbar puncture. 7. Patients who are taking α2 adrenergic agonist or antagonists. 8. Pre existing severe cardiac disease, heart block/dysrhythmias. 9. Contraindications to subarachnoid block.(Duration of study is around one year)
研究者
研究点 (1)
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