GnRH Agonist (GnRHa) Withdrawal at Late Stage of Long Protocol and the Incidence of Ovarian Hyper-stimulation
Infertile High-risk Patients With Polycystic Ovaries
About this trial
This is an interventional prevention trial for Infertile High-risk Patients With Polycystic Ovaries focused on measuring GnRH agonist withdrawal, OHSS, E2, VEGF
Eligibility Criteria
Inclusion Criteria:
ninety-six infertile patients with PCOs (12 or more follicles 2-9 mm in diameter were detected in ovaries by ultrasound detection) undergoing IVF treatment were enrolled.
Exclusion Criteria:
the subjects included the followings: a basal FSH level of > 10IU/L; age >35 years; a body mass index (BMI) > 30 kg/m2; ovarian surgery radiotherapy or chemotherapy; ovarian dysfunction; endometriosis; hyperprolactinemia; thyroid dysfunction; the presence of organic pelvic diseases.
Sites / Locations
- Research Room of Reproductive Medicine, The Outpatient Building of Drum Tower HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
GnRH agonist withdrawal
control group
All the patients received a midluteal long GnRH agonist (GnRH-a) and a gonadotropins (recombinant FSH) stimulation protocol. When the diameter of one or more follicles was ≥ 14 mm, GnRHa (0.05mg/d) was withheld in the study group.
All the patients received a midluteal long GnRH agonist (GnRH-a) and a gonadotropins (recombinant FSH) stimulation protocol. In the control group, GnRHa (triptorelin, 0.05mg/d,)was used to the day of ovulation trigger.