PACTR202202641392530尚未招募3 期
Comparison of the efficacy of oral Dydrogesterone with Micronized vaginal progesterone for luteal phase support in women undergoing In vitro fertilization (IVF) at the Federal Medical Centre Abuja: a randomized clinical trial
Researcher0 个研究点目标入组 300 人开始时间: 2022年1月6日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 300
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •Signed informed consent
- •Premenopausal females, age = 19 years = 44 years
- •Non-smokers
- •Normal follicular phase (Day 2-4) hormones (FSH, LH, E2, PRL, T, and TSH
- •Documented history of infertility
- •Normal endovaginal ultrasound at screening
- •Subject is not pregnant
- •Clinically indicated protocol for induction of IVF with a fresh embryo
- •Single or dual embryo transfer
- •BMI = 18 and = 30 kg/m2
排除标准
- •Evidence of diseases which could limit participation in or completion of the study
- •Acute urogenital disease
- •Known allergic reactions to progestogens
- •Intake of any other experimental drug or on going treatment of any illness
- •participation in any other clinical trial within 30 days prior to study start
- •Disability or any condition leading to lack of fitness to participate in or to complete the study
- •Current or recent substance abuse, including alcohol and tobacco
- •History of chemotherapy or radiotherapy
- •Patients with more than 3 unsuccessful IVF attempts
- •Women in whom pregnancy is contraindicated
- •Refusal or inability to comply with the requirements of the study protocol for any reason
- •History of recurrent pregnancy loss
研究者
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