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临床试验/IRCT20201126049497N1
IRCT20201126049497N1招募中2 期

Comparison the effect of 3 days with 7 days GNRH-antagonist in prevention of ovarian hyperstimulation syndrome(OHSS) in women undergoing assisted reproductive technology (ART)

Birjand University of Medical Sciences0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
入组人数
40

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 40 years(—)
性别
Female

入选标准

  • Having informed consent to enter the study.
  • The possibility of useful intervention on individuals.
  • Age between 18 and 40 years.
  • The person is at risk for OHSS syndrome (for example, the number of recovered eggs is more than 15 or serum estradiol more than 3000 pg / ml
  • Any person who does not meet any of the exclusion criteria will be included in the study if satisfied

排除标准

  • Dissatisfaction to enter the study
  • Age less than 18 years or more than 40 years
  • Any disease that interferes with the intended intervention.
  • Patient with diabetes / hemophilia or coagulation disorde
  • Patients with pulmonary fibrosis, swelling or inflammation around the heart or lungs, high blood pressure, liver disease, heart valve disease, or allergy to cabergoline or ergot derivatives
  • Use of drugs that affect the development of OHSS syndrome (calcium gluconate / metformin / letrozole / other GNRH-ant antagonists)
  • Pregnancy during the study cycle
  • Contraindications that are considered by a specialist and are not included in the test.

研究者

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