CTRI/2024/04/064994尚未招募Unknown
A Real-world study to evaluate the Reproductive outcomes and Safety Profile in patients treated with Dydrogesterone for Luteal Phase Support in ART: A Prospective Observational Study - Not Applicable
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •? Female patients of age = 21 years.
- •? Patients who are legally married
- •? Patients who require Luteal Phase Support during the Assisted reproductive techniques (ART)
- •? Patients who are prescribed Dydrogesterone as part of routine clinical practice as determined by the Investigator.
- •? Patients or their legally representatives who are willing provide written informed consent to participate in the study and are willing to adhere to the study procedures as per the protocol.
排除标准
- •? Patients with known severe liver or severe kidney or liver
- •dysfunction at the time of initiation of trial
- •? Patients who are allergic to Dydrogesterone
- •? Participation in another study concurrently or within 4 weeks
- •before initiation of trial.
- •? Presence of any other clinically significant disease or laboratory findings that in the Investigators opinion may
- •affect the study outcome parameter data.
研究者
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