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临床试验/IRCT2015092513336N2
IRCT2015092513336N2已完成未知

Comparison Apotel and suppositories diclofenac on pain relief after cesarean section among primiparous women

Research Council of Mashhad University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
120

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
no limit 至 no limit(—)
性别
Female

入选标准

  • minimum education subjects as reading and writing, lives with his wife, a singleton pregnancy, gestational age 38 to 42 weeks, primiparous women, healthy baby and the first minute Apgar score 7-10, the same method cesarean delivery and a cross-section (skin and uterus), mothers with vital signs are favorable. Exclusion criteria: The presence of unusual complication of surgery (bladder trauma or other injury during surgery), preoperative fever, Smoking and drug addiction, hysterectomy Associated with cesarean, suffering from medical disorders (diabetes, hypertension, heart disease and vascular, renal, pulmonary, gastrointestinal, thyroid, immune disorders, infectious, psychiatric, metabolic disorders, electrolyte and irritable bowel syndrome), sensitivity to paracetamol, liver and kidney function decline, chronic alcoholism, chronic malnutrition or dehydration, taking probenecid or Sylasyd year or drugs are enzyme induction.

排除标准

  • 未提供

研究者

发起方
Research Council of Mashhad University of Medical Sciences

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