NCT04172727已完成4 期
Subarachnoid Block With Ultrasound-Guided Transversalis Fascia Plane Block for Cesarean Sections: A Randomized Placebo-Controlled Double-Blind Study
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
- 60
- 试验地点
- 1
- 主要终点
- opioid consumption
研究概览
简要总结
Postoperative pain management is critical for the fulfillment of the maternal duties. The transversalis fascia plane (TFP) block provides adequate postoperative analgesia in the T12 and L1 dermatomes. The aim of this study was to investigate the effect of the TFP block on postoperative opioid consumption and pain scores in patients undergoing cesarean section (CS) under spinal anesthesia.
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, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 45 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •aged between 18 and 45
- •American Society of Anesthesiologists (ASA) physical score I or II
排除标准
- •Patients who received general anesthesia
- •hypersensitivity to the agents to be used
- •body mass index (BMI) greater than 35 kg/m2
- •coagulopathy
- •local infections
- •opioid addiction
- •pregnancy-related hypertension or diabetes mellitus
研究组 & 干预措施
ultrasound guided transversalis fascia plane block
Active Comparator
20 mL of 0.25% bupivacaine
干预措施: Bupivacaine Hcl 0.25% Inj (Drug)
ultrasound guided sham block
Placebo Comparator
20 mL of saline
干预措施: saline 0.9% (Drug)
结局指标
主要结局
opioid consumption
时间窗: Postoperative first 24hour
morphine consumption first 24hour
次要结局
- pain scores(postoperative 0-24 hours)
研究者
Ali Ahiskalioglu
Principal Investigator
Ataturk University
研究点 (1)
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