CTRI/2024/12/077606尚未招募4 期
A clinical prospective double blinded randomized controlled study to compare the intrathecal ropivacaine and dexmedetomidine with intrathecal ropivacaine in infraumblical surgeries.
pacific medical college and hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年12月16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
- 80
- 试验地点
- 1
- 主要终点
- -Duration of analgesia
研究概览
简要总结
To assess safety and efficacy of intrathecal Heavy inj.Ropivacaine (3ml) plus
Dexmedetomidine (7mcg) versus a combination of intrathecal Heavy inj.Ropivacaine
(3ml) and normal saline
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
- •Age group 18–60 years of either sex.
- •ASA physical status 1 and
- •Patients posted for Infraumbilical surgeries.
排除标准
- •The following criteria were excluded from the study:
- •Patient refusal.
- •Patients with contraindication to spinal anaesthesia.
- •Patients with any systemic disease.
- •Allergy to either drug used in the study.
- •History of substance abuse.
结局指标
主要结局
-Duration of analgesia
时间窗: 24 MONTHS
-Post operative analgesic requirement
时间窗: 24 MONTHS
-Side effects if any
时间窗: 24 MONTHS
-VAS score
时间窗: 24 MONTHS
次要结局
- Duration of analgesia(Side effects if any)
研究者
Robin Arora
Pacific Medical College and Hospital Udaipur
研究点 (1)
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