CTRI/2022/09/045531尚未招募不适用
"Comparison of analgesic effect of Clonidine as adjuvant with 0.35% concentration of Ropivacaine in USG guided thoracic Paravertebral block in modified radical Mastectomy: A prospective randomized double blind Study"
Department Of Anaesthesia RNT Medical College udaipur1 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2022年9月20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
- 78
- 试验地点
- 1
- 主要终点
- DURATION OF ANALGESIA
研究概览
简要总结
The purpose of this trial to find out minimum concentration of ropivacaine with clonidine for better Post operative analgesia in modified redical mastectomy
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Double Blind Double Dummy
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- Female
入选标准
- •Patients who are 18-60 year of age, ASA grade I and II, Normotensives or treated Hypertensives who will undergo MRM surgery will be included in the study.
排除标准
- •Patient refusal,Patients with ASA III and higher,Patient having allergy to study drugs, Coagulation disorders,History of cardiovascular disease, Uncontrolled blood pressure,Pregnancy.
结局指标
主要结局
DURATION OF ANALGESIA
时间窗: up to 24 hrs after completion of surgery
次要结局
- THE RESCUE ANALGESIC REQUIREMENT(OVER FIRST 24 HRS POSTOPERATIVELY)
研究者
研究点 (1)
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