Rescue Progesterone Supplementation in Patients With Low Progesterone on the Day of Embryo Transfer for Artificial Endometrial Preparation Cycles: a Non-inferiority Study
试验速览
- 阶段
- 2 期
- 状态
- 暂停
- 发起方
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Evaluate the ongoing pregnancy rate
研究概览
简要总结
Endometrin is a progesterone supplement prescribed during in vitro fertilization (IVF) for preparation for embryo transfer. The usual dose of Endometrin is 100 mg two to three times per day in the form of an effervescent tablet to be inserted vaginally.
The purpose of this research project is to evaluate the dose response of the Endometrin when determined based on the blood level of progesterone on the day of the FET. According to the literature, a predefined level of progesterone in the blood should be reached in order to have favorable conditions for pregnancy. The hypothesis being that a woman with low progesterone levels would benefit from a dose of Endometrin of 600 mg (200 mg 3x/day) to decrease the risk of miscarriage and improve the chances of pregnancy. Women with adequate progesterone levels according to the literature, would continue with the standard dose of progesterone prescribed at clinique ovo which is 300 mg (100 mg 3x/day).
PIBF (Progesterone Induced Blocking Factor) levels, a protein found in the blood that could also predict pregnancy outcomes in women using IVF will also be looked at.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 42 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women 18-42 years of age
- •Normal uterine cavity (according to treating physician)
- •FET substituted cycle prescribed
- •First or second cycle of FET
- •Adequate endometrial pattern (triple layer) and thickness (>7 mm) after adequate standard endometrial preparation in artificial cycle
排除标准
- •Any uterine abnormalities confirmed by treating physician making participant unable to proceed with FET
- •Patients with personalized FET according to the endometrial receptivity assay tests
- •Previous allergic reactions to progesterone or any of the ingredients of Endometrin
- •Severe hepatic dysfunction or disease
- •Known or suspected breast cancer or genital tract cancer
- •Known active arterial or venous thromboembolism or severe thrombophlebitis or cerebro-vascular disease, or a history of these events
- •Diagnosed porphyria
- •Undiagnosed abnormal vaginal bleeding
- •Known missed abortion or ectopic pregnancy
- •Recurrent pregnancy loss excluding biochemical pregnancies
- •Hypersensitivity to Acetylsalicylic acid (ASA), salicylates, non-steroidal anti-inflammatory drugs (NSAIDs), analgesics, antipyretics or other ingredients in the product or component of the container
- •Acute gastrointestinal ulcer, history of gastrointestinal ulcers and hemorrhagic diathesis
- •Active or severe renal disease, or congestive heart failure
- •History of asthma induced by salicylates or other NSAIDs
- •Use of methotrexate at doses of 15mg/week or more
- •Glucose-6-phosphate dehydrogenase (G6PD) deficiency
研究组 & 干预措施
Endometrin 100 mg three times per day (TID)
Women with progesterone levels ≥ 8.8 ng/ml during frozen embryo transfer cycle will take Endometrin 100 mg TID until 10th week of pregnancy
干预措施: Progesterone Effervescent Vaginal Tablet (Drug)
Endometrin 200 mg three times per day (TID)
Women with progesterone levels < 8.8 ng/ml during frozen embryo transfer cycle will take Endometrin 200 mg TID until 10th week of pregnancy
干预措施: Progesterone Effervescent Vaginal Tablet (Drug)
结局指标
主要结局
Evaluate the ongoing pregnancy rate
时间窗: 6 to 8 weeks after Frozen Embryo Transfer
Viability ultrasound
次要结局
- Evaluate the miscarriage rate(6 to 8 weeks after Frozen Embryo Transfer)
- Evaluate progesterone levels(Before embryo transfer and 10 days after embryo transfer)
- Evaluate the rate of biochemical pregnancy(10 days after frozen embryo transfer)