drugset / Trial / NCT02418533

Mono-menotropins Versus rFSH Protocol on Embryo Quality

NCT02418533

Completed 109 enrolled Main Line Fertility Center
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is for couples pursuing in vitro fertilization (IVF) with preimplantation genetic screening (PGS) of embryos to achieve pregnancy. The objective of this clinical trial is to study the effect of mono-menotropins for COS versus recombinant follicle stimulating hormone (rFSH) on cleavage-stage and blastocyst embryo quality after IVF. Embryo quality parameters include conventional embryo grade, early embryo viability assessment (Eeva) time-lapse parameters, and chromosomal aneuploidy rates after PGS. This pilot study is expected to significantly contribute to optimization of treatment regimens and stimulation protocols to optimize embryo quality.

Timeline

Start
2015-03
Primary completion
2017-04
Completion
2017-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Gonal-f Protein / enzyme biologic 300 iu Subcutaneous
Subject Gonal-f Protein / enzyme biologic 375 iu Subcutaneous
Subject Gonal-f Protein / enzyme biologic 450 iu Subcutaneous
Subject Menopur Protein / enzyme biologic 300 iu Subcutaneous
Subject Menopur Protein / enzyme biologic 375 iu Subcutaneous
Subject Menopur Protein / enzyme biologic 450 iu Subcutaneous

Indications