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)
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.
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