EUCTR2017-004797-33-BE进行中（未招募）1 期
The efficacy of continuous ropivacaine wound infusion after cesarean delivery in pain management.
CHU Tivoli0 个研究点目标入组 68 人开始时间: 2018年4月4日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 68
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Inclusion criteria will be all patients undergoing cesarean delivery with
- •- a gestation of 34 weeks or more
- •- American Society of Anesthesiology (ASA) I or II
- •- = age 18 years
- •- signed informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 68
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Exclusion criteria will be
- •- allergies to used analgesics
- •- ASA III or higher
- •- pre- or eclampsia
- •- diabetes mellitus type I or II
- •- postpartum hemorrhage (defined as = 1 L blood loss)
- •- BMI = 35
- •- preoperative opioid consumption/abuse
- •- psychiatric disorders
- •- patient refusal to participate
- •- language barrier
研究者
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