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临床试验/IRCT20230725058918N1
IRCT20230725058918N1招募中3 期

Comparing the effects of red and near-infrared light diode radiation with acupressure on pain intensity and length of the first stage of labor in primiparous women

Mashhad University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
90

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 years 至 35 years(—)
性别
Female

入选标准

  • A pregnant mother aged 18-35 must be primiparous, single, and Iranian.
  • Have a fetus with cephalic presentation with a gestational age of 37-41 (based on LMP or ultrasound of the first trimester of pregnancy).
  • Having literacy in reading and writing and the absence of speech and hearing problems that prevent communication with the interventionist.
  • Signed the written consent form.
  • The estimated weight of the fetus (based on Johnson criteria or third trimester ultrasound) should be between 2.5-4 kilos.
  • Cerebral-pelvic disproportion and fetal anomaly have not been diagnosed.
  • The onset of labor should be spontaneous based on 4 cm dilation and regular uterine contractions.
  • Absence of drug and alcohol addiction, as well as not having used narcotics for 8 hours before the intervention.
  • Do not have medical diseases.
  • Do not have obstetric complications.
  • Do not have a history of surgery on the uterus or cervix.
  • Do not have lesions such as wounds, scratches, burns, eczema, or other lesions on the skin that prevent light therapy.

排除标准

  • In case of any obstetric complications such as bleeding and fetal heart rate disorders, the pregnant mother will not be included in the study.

研究者

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