The Effect of RECO-18 on Infertile Women Undergoing in Vitro Fertilization-embryo Transfer
Fertility Disorders, Infertility, Female
About this trial
This is an interventional treatment trial for Fertility Disorders focused on measuring pregnancy rate, in vitro fertilization-embryo transfer
Eligibility Criteria
Inclusion Criteria:
- female, 20 to 40 years old
- the 1st or 2nd cycle of IVF/ICSI treatment
- BMI≤30Kg/m2
- with bilateral ovaries
- be eligible for IVF/ICSI treatment
Exclusion Criteria:
- Repeated implantation failures (with previous 3 or more IVF/ICSI failures)
- moderate to severe endometriosis
- untreated hydrosalpinx
- untreated endometrial disease
- contraindications for assisted reproductive techniques or gestation
- a history of ovarian surgery
- expected poor ovarian response (POR) or previous POR
- polycystic ovarian syndrome
- participants in clinical trials of other drugs within one month prior to enrollment; • hypersensitivity to follicle-stimulating hormone α, FSH, human menopausal gonadotropin, LH or excipients
- uncontrolled endocrine diseases (such as hyperthyroidism, hypothyroidism, adrenal gland disease, obesity, etc.)
- percutaneous epididymal sperm aspiration or testicular sperm aspiration
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Control group
Treatment group
The control group takes the multi-vitamins (Elevit, Bayer S.A.) with the dosage of one tablet per day on the 1st to 5th day of menstruation, then perform ovulation induction on the second menstrual cycle, and continue to take multi-vitamins until the day of oocyte retrieval.
The treatment group begins to take Reco-18 on the 1st to 5th day of menstruation with a dosage of 4 pills per day for the whole menstrual cycle, then perform ovulation induction on the second menstrual cycle, and continue to take Reco-18 until the day of oocyte retrieval.