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临床试验/IRCT20110524006582N37
IRCT20110524006582N37招募中3 期

The effect of topical ointment of Propolis on severity of episiotomy pain and wound healing: a randomized controlled trial

Tabriz University of Medical Sciences0 个研究点目标入组 72 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
72

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

  • Gravid one and two women
  • Living in Tabriz city
  • Willingness and possibility of the mother to go to Alzahra and Taleghani hospitals on the 10th day
  • Vaginal delivery with mediolateral incision

排除标准

  • Prolonged rupture of the amniotic sac (more than 18 hours)
  • Use of special drugs such as anti-inflammatory and anticoagulant drugs
  • Addiction to alcohol or drugs
  • History of diseases interfering with wound healing such as systemic, cardiac, renal, pulmonary diseases, coagulation disorder, immunodeficiency, connective tissue disorder, diabetes, anemia, mental illness, hemophilia (based on medical records)
  • Abnormal postpartum bleeding
  • Preterm labor
  • Allergy to propolis
  • Large or extended episiotomy (third or fourth degree tear and episiotomy cut length greater than 3-4 cm)
  • History of surgery or visible lesions in the perineum
  • Severe anemia (hemoglobin less than 7 grams per deciliter)
  • Other tears in addition to episiotomy, such as urethral tears
  • Non-continuing cooperation of participants
  • Incomplete participation that is not possible to achieve results

研究者

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