CTRI/2022/11/047511尚未招募未知
A prospective, observational study to compare the patient reported outcomes with the use of oral dydrogesterone vs. micronized vaginal progesterone in high risk pregnancies (PERCEPT study) - PERCEPT
试验速览
- 阶段
- 未知
- 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
- •1.Pregnant women with age of >= 18 years and who are ready to give informed consent for participation in the study.
- •2.Women with clinically diagnosed pregnancy of <= 12 weeks of gestation and visiting department of obstetrics and gynecology.
- •3.History of more than two miscarriages and/or presenting with vaginal bleeding
- •4.Patient suitable for treatment with micronized vaginal progesterone or dydrogesterone therapy based on locally approved prescribing information.
排除标准
- •1.Pregnant women who have contraindications for use of micronized vaginal progesterone or dydrogesterone.
- •2.Any condition that, in the opinion of the investigator, does not justify the patientâ??s inclusion in the study.
研究者
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