drugset / Trial / NCT02827656

Comapring Luteal Phase Support in IVF Patients Who Are at High Risk for Developing OHSS

NCT02827656

Unknown 50 enrolled Meir Medical Center
RandomizedParallel-groupSingle-blindTreatment

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..

Timeline

Start
2016-08
Primary completion
2017-08
Completion
2017-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Decapeptyl Unknown 0.1 mg Subcutaneous
Comparator human chorionic gonadotropin Protein / enzyme biologic 50 ug Subcutaneous

Indications