Comapring Luteal Phase Support in IVF Patients Who Are at High Risk for Developing OHSS
Status:
Unknown status
Trial end date:
2017-12-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to compare two luteal support protocols in In vitro
fertilization patients (IVF) and are at risk of developing ovarian hyperstimulation syndrome
(OHSS). We would like to determine whether luteal Decapeptyl on days 3, 6,9 post ovulation
triggering is as good as low dose hCG on day 3 post triggering..