NCT01516268已完成4 期
the Effect of Adding Sufentanyl to Bupivacaine in Transversus Abdominis Plane (TAP) Block Under the Guide of Ultrasound to Reduce the Narcotic Dosage, Side Effects and Pain in the First 24 Hours After Cesarean Delivery
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Narcotic Dosage
研究概览
简要总结
Adding sufentanyl to bupivacain in Transversus Abdominis Plane (TAP) block under ultrasound guide can reduce narcotic dosage, side effects and pain after cesarean delivery.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •female 18 to 40 Years
- •class ASA 1 and 2
- •candidates for elective cesarean section
排除标准
- •renal failure
- •liver failure
- •cardiac disorder
- •coagulopathy
- •hepatomegaly
- •splenomegaly
- •drug sensitivity and abuse
- •morbid obesity
- •history of post operative nausea and vomiting
- •motion sickness
- •local hypoesthesia
研究组 & 干预措施
Sufentanyl group
Active Comparator
IN case group we add 1cc sufentanyl to 20 cc bupivacain in TAP block
干预措施: Sufentanyl (Drug)
Control group
Placebo Comparator
In control group we add 1cc salin to 20cc bupivacain in TAP block
干预措施: Sufentanyl (Drug)
结局指标
主要结局
Narcotic Dosage
时间窗: over 24 hours after surgery
The total dosage of morphin consumed by the patients in sufentanil or control group.
次要结局
- Pain(24h)
研究者
Laleh Eslamian
Associated Prof.MD
Tehran University of Medical Sciences
研究点 (1)
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