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临床试验/IRCT20211024052856N1
IRCT20211024052856N1招募中未知

Evaluation of the effect of using abdominal binder on the amount of vaginal bleeding, pain intensity and mobility after cesarean section

Esfahan University of Medical Sciences0 个研究点目标入组 184 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
184

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

  • Spinal anesthesia
  • Do not use anti-anxiety and hypnotic drugs and painkillers
  • No underlying disease (neuromuscular disorders, hypertension, kidney disease, heart disease)
  • BMI between 18/5 to 29/5
  • Uncomplicated pregnancy such as absence of eclampsia and preeclampsia
  • Do not have any coagulation disorders or use anticoagulants
  • Pfannenstiel incision on the skin and kerr incision on the uterus

排除标准

  • Intolerance of the abdominal binder by the patient
  • Reluctance to continue participating in the study
  • Severe postoperative bleeding
  • Damage to body tissues during cesarean section such as damage to the urinary tract and gastrointestinal tract

研究者

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