CTRI/2017/02/007897已完成不适用
A study on pain and quality of life among women after breast surgery and comparison of two techniques of analgesia.
All India Institute of Medical Sciences Bhubaneswar Intramural grant1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年1月7日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Quality and duration of analgesia
研究概览
简要总结
To Compare block characteristics, complications and quality of life in patients undergoing breast surgery under usg guided nerve block. The patients will be given nerve block under sedation and spontaneous ventilation, with avoidance of opioid medications.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 19.00 Year(s) 至 99.00 Year(s)（—）
- 性别
- All
入选标准
- •Adult patients undergoing breast surgery ( MRM).
排除标准
- •Allergy to LA agent.
结局指标
主要结局
Quality and duration of analgesia
时间窗: Need for opiate rescue, Duration to first request for (non opiate analgesic), VAS scores for first 24 hours post surgery pain scores will be assessed at 0, 30 min, 1 hr, 2 hr and 2nd hrly thereafter at rest and on arm movement. | the total amount of analgesic consumed at end of 24 hrs post op will be assessed .
次要结局
- Complications of Block(Opioid REquirement)
研究者
研究点 (1)
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