临床试验/CTRI/2024/09/073926

CTRI/2024/09/073926尚未招募不适用

Comparison of analgesic efficacy of Dexmedetomidine with Bupivacaine v/s Bupivacaine alone in pecto-intercostal fascial plane block in adult patient undergoing median sternotomy: A randomized control trial

AIIMS PATNA1 个研究点分布在 1 个国家目标入组 70 人开始时间: 2024年9月20日最近更新: 2024年9月3日

试验速览

阶段: 不适用
状态: 尚未招募
发起方
入组人数: 70
试验地点: 1
主要终点: measure the time to first rescue analgesia post-operative in either of groups.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Comparison of analgesic efficacy of Dexmedetomidine with Bupivacaine v/s Bupivacaine alone in pecto-intercostal fascial plane block in adult patient undergoing median sternotomy: A randomized control trial-

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: Participant and Investigator Blinded

入排标准

年龄范围: 18.00 Day(s) 至 70.00 Day(s)（—）
性别: All

入选标准

•ASA physical status: I.
•Age: 18-70 years.

排除标准

•Patient refusal to participate in the study
•Duration of surgery more than 5 hours
•Hypersensitivity, or a history of Local Anesthetic allergies
•Undergone emergent or redo surgeries
•Cognitive dysfunction.

结局指标

主要结局

measure the time to first rescue analgesia post-operative in either of groups.

时间窗: measure the time to first rescue analgesia post-operative in either of groups.

次要结局

1) Total opioid consumption in 24 hours(2) Time to extubation)

研究者

发起方

AIIMS PATNA

申办方类型

Government medical college

责任方

Principal Investigator

主要研究者

Shashi Kant

AIIMS, Patna

研究点 (1)

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