跳至主要内容
临床试验/IRCT2017062633812N2
IRCT2017062633812N2已完成2 期

Investigating the effect of Commiphora mukul cream on improvement of breast engorgement of women referred to the health center of Kerman University of medical science in 2015-2016

Vice Chancellor for research Shahid Beheshti University of Medical Sciences0 个研究点目标入组 105 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
105

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
15 years 至 45 years(—)
性别
Female

入选标准

  • The study inclusion criteria for the Iranian; literate mothers
  • who were in the 1st to 15th days after delivery consisted of having
  • breast engorgement with a minimum intensity score of 2 based
  • on the checklist (with a maximum score of 19); A sublingual temperature
  • below 38 ° C; Having had engorgement symptoms during the first
  • 15 days after delivery; No use of medications for stopping breastfeeding;
  • No use of topical herbal therapies; Not having developed breast
  • abscess or mastitis; No prohibition on lactation; No history of any
  • allergies to Commiphora mukul or other plants; And nursing every 2 to 3 hours.
  • For the neonates, the inclusion criteria consisted of being a singleton
  • and having a full-term birth and normal birth weight (2500-4000 g);
  • Being able to suck on nipples; Not being prohibited from breastfeeding;
  • ?And demanding to be nursed every 2 to 3 hours. The study exclusion criteria for the mothers consisted of the incidence of allergy to Commiphoramukul; A general temperature exceeding 38 ° C after beginning the intervention; Use or need to antiinflammatory medications or painkillers or warm compress or cold compress or acupressure interfering with the designed intervention during the course of the study; And the incidence of unexpected events for either participants interfering with their breastfeeding; Use of the proposed treatment less than five times a day. The infants were excluded from the study if they lost the study inclusion criteria for any reason, including getting a fever during the
  • course of the intervention.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research Shahid Beheshti University of Medical Sciences

相似试验