Effects of SNP of GnRH Receptor Genes in IVF Patients
Infertility, Female
About this trial
This is an interventional screening trial for Infertility, Female focused on measuring single nucleotide polymorphism,GnRH receptor, IVF
Eligibility Criteria
Inclusion Criteria:
- regular periods of spontaneous menstruation (23~35 days)
- basal serum FSH <12 IU/L
- use of short-acting GnRH-a long protocol for pituitary down-regulation.
Exclusion Criteria:
- polycystic ovary syndrome (PCOS)
- hypothalamic-pituitary lesions
- use of oral contraceptives
- treated with a GnRH-a within 3 months before the start of GnRH-a treatment for this study
- failure to sign informed consent form.
Sites / Locations
Arms of the Study
Arm 1
Experimental
triptorelin
GnRH-a will be given everyday to the patient undergoing IVF treatment from middle luteal phase to the day of HCG. After 14 days of injection, serum FSH/LH/E2 will be checked. Then ovarian stimulation will be started by giving daily subcutaneous injection of recombinant FSH 150~300 IU. An appropriate dose of HMG (75~150 IU) will be added when follicles are larger than 12~14mm in diameter. When one leading follicle is >18mm in diameter, or two follicles are >17mm in diameter, or three follicles are >16mm in diameter, final ovulation will be triggered by a single injection of HCG 4,000~10,000 IU or Ovidrel® 250μg (equivalent to HCG 6,500 IU)