The Efficacy of Ultrasound-guided Transversus Abdominis Plane ( TAP) Block Versus Standard Analgesic Protocol for Postoperative Analgesia After Elective, Cesarean- Section Delivery- A Randomize Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Pain Score
研究概览
简要总结
Relief from pain is part of the fundamental human right to health. (1) However, available evidence indicates an increasingly detailed understanding of the pathophysiology of pain and general inadequacy of its treatment.
详细描述
Background: Relief from pain is part of the fundamental human right to health. (1) However, available evidence indicates an increasingly detailed understanding of the pathophysiology of pain and general inadequacy of its treatment.
Rationale: Assessment and Improving the Pain Management Modality
Study objectives: In this study, determined the efficacy of TAP block in patients undergoing cesarean section.
Methods:
This study is a cross-sectional study. It is a multi-centric study as it was conducted in different Governmental hospitals.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Age: 20-50 years
- •Patients of >50 kg or <100 kg weight.
- •Urgency: Elective, Emergent and Urgent cases
排除标准
- •Patients of <50 kg or >100 kg weight
- •Any contraindication to any of anesthesia medications
- •Patient unable to understand numeric rating scale (NRS)
研究组 & 干预措施
Group A,
women who received TAP block.
干预措施: TAP block (Procedure)
Group B
Received Usual modality of analgesics (Paracetamol, Tramadol, and Pethidine).
干预措施: TAP block (Procedure)
结局指标
主要结局
Pain Score
时间窗: 24 hours
NRS
次要结局
未报告次要终点
研究者
Mohammed Abaalkhayl
Associate Proffesor
Qassim University