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临床试验/CTRI/2025/04/084113
CTRI/2025/04/084113尚未招募4 期

A Prospective randomized and double blinded study comparing duration of post operative analgesia between ultrasound guided Interscalene block with Ropivacaine 0.5 percent and Interscalene block with Ropivacaine 0.5 percent and Dexmedetomidine as adjuvant for shoulder arthroscopic surgeries done under General anesthesia

SRM institute of medical sciences1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年4月20日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
To study the postoperative analgesia in Group A and B

研究概览

简要总结

USG guided interscalene block for patients posted for shoulder arthroscopic surgery in SIMS hospital

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
20.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • ASA Grade 1 and 2 Patients admitted for shoulder arthroscopic surgery.

排除标准

  • ASA grade 3 and 4 Pregnant and lactating mothers.

结局指标

主要结局

To study the postoperative analgesia in Group A and B

时间窗: 30 minutes, 2 hours, 6 hours, 18 hours, 24 hours, 36 hours, 48 hours

次要结局

  • To study the motor weakness & rescue analgesic requirement(30 minutes 2 hours 6 hours 18 hours 24 hours 36 hours 48 hours)

研究者

发起方
SRM institute of medical sciences
申办方类型
Private hospital/clinic
责任方
Principal Investigator
主要研究者

Dr Aravindh Veeresh

SRM institute of medical sciences

研究点 (1)

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