drugset / Trial / NCT02215135

Corifollitropin Alfa Application in PCOS Patients

NCT02215135

Phase 4 Unknown 30 enrolled Shin Kong Wu Ho-Su Memorial Hospital
NaSingle-groupOpen-labelTreatment

Summary

Corifollitropin alfa, single dose administered sustains multiple follicular development for 7 days. However, It may induce ovarian hyperstimulation syndrome (OHSS), especially in high responder women such as patients of polycystic ovary syndrome (PCOS). In GnRH antagonist protocol with agonist triggering of final oocyte maturation, following embryo cryopreservation can almost eliminate the risk of OHSS. To decrease the injection burden and prevent OHSS in PCOS patients undergoing IVF treatment, ovarian hyperstimulation with Corifollitropin alfa in GnRH antagonist protocol and GnRH agonist triggering of final oocyte maturation, following elective embryo cryopreservation was designed in this study. The purpose of this trial was conducted to confirmed whether this novel protocol could prevent OHSS, decreased the injection burden of PCOS patients and single dose corifollitropin alfa could support multiple follicular growth for 7 days.

Timeline

Start
2014-01
Primary completion
2015-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Corifollitropin alfa Protein / enzyme biologic 100 ug Subcutaneous
Subject Corifollitropin alfa Protein / enzyme biologic 150 ug Subcutaneous

Indications

No indication recorded.