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临床试验/CTRI/2026/04/108801
CTRI/2026/04/108801尚未招募不适用

Efficacy of adjuvant effect of intravenous vs intrathecal dexmedetomidine on 0.5%Hyperbaric levobupivacaine for postoperative analgesia in patients undergoing lower abdominal and lower limb surgeries under Subarachnoid block- a prospective double blinded randomised controlled study

The Dean1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2026年5月3日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
75
试验地点
1

研究概览

简要总结

Analysis of safety profiles and side effects.

• Recommendations on optimal dexmedetomidine administration route.

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 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients under American society of Anaesthesiologist classification of class I & II Posted for elective lower abdominal and lower limb surgeries.

排除标准

  • Coagulation abnormalities Bleeding disorder Spine deformity Cardiac /renal disease Drug allergy.

研究者

发起方
The Dean
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Priyanka Sakthivel

Chettinad hospital and research institute

研究点 (1)

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