PACTR201506001145361已完成未知
Evaluation of post-cesarean pain After Intraperitoneal Lidocaine Instillation versus intravenous lidocaine
benha university hospital0 个研究点目标入组 110 人开始时间: 2015年5月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 110
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Year(s) 至 40 Year(s)（—）
- 性别
- Female
入选标准
- •1-Singleton pregnancy,
- •2-more than or equal completed 37 gestational weeks,
- •3-indicated to undergo elective cesarean delivery for various indications e.g., primigravida with breech presentation, macrosomia, intrauterine growth restriction and contracted pelvis,
- •4-willing to participate in the study.
排除标准
- •1-extreme of age (below 18 ¿ above 40 year),
- •2-uncooperative patients,
- •3-previous abdominal scars, including previous cesarean or myomectomy, multiple gestation,
- •4-BMI >35 kg/m², chorioamnionitis, hypersensitivity or contraindications to lidocaine,
- •5-bronchial asthma,
- •6-bleeding diathesis,
- •7-pregnancy induced-hypertension,
- •8-liver or kidney diseases,
- •9-diabetes mellitus,
- •9-patients with psychological disturbance, 10-any form of chronic pain before or during pregnancy
研究者
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