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临床试验/CTRI/2021/01/030357
CTRI/2021/01/030357已完成不适用

The Effect of Adding Epinephrine To Combination of 0.5% Hyperbaric Bupivacaine and Dexmedetomidine in Intrathecal Anaesthesia- A Prospective, Double Blinded Randomized Control Study

NOT APPLICABLE1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年1月13日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
1
主要终点
Duration of analgesia

研究概览

简要总结

This study is designed to evaluate intrathecal anesthesia and postoperative analgesia of adding epinephrine to a combination of 0.5% hyperbaric bupivacaine and dexmedetomidine.

Dexmedetomidine, a highly selective α2 adrenergic agonist increases the duration of anesthesia & analgesia whereas Epinephrine, a vasoconstrictor, reduces the systemic toxicity by decreased absorption of local anesthetics into the bloodstream and extends the duration of anesthesia.

We are expecting that the decrease in heart rate and blood pressure with a combination of bupivacaine and dexmedetomidine is balanced by adrenaline as it increases the same resulting in prolonged anesthesia with better hemodynamic status.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
15.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • ASA GRADE 1 AND 2 LOWER LIMB SURGERIES WITH PROBABLE DURATION OF 2 HOURS.

排除标准

  • Patients refusal Contraindication to regional anesthesia Coagulopathy History of significant coexisting diseases (IHD, impaired renal functions, and severe liver disease) Chronic alcoholics and malnourished patients Atrioventricular block, incomplete or partial heart blocks, or intake of beta blockers.

结局指标

主要结局

Duration of analgesia

时间窗: EVERY 15 MINUTES POST OPERATIVELY

次要结局

  • Duration of sensory block & motor block(EVERY 15 MINUTES POST OPERATIVELY)

研究者

申办方类型
Other [NOT APPLICABLE ]

研究点 (1)

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