Condition: Ovarian Stimulation · Quality of Life · Preimplantation Genetic Testing · Sponsor: University Hospital, Ghent
P-CCROSS is a randomized, prospective monocentric phase 4 study with a crossover study design. The aim of the study is to compare patient satisfaction (by means of questionnaires) and treatment compliance with IVF treatment with CFA (corifollitropin alfa) and PPOS (Progestin-Primed Ovarian Stimulation) versus conventional IVF treatment with a recombinant FSH/GnRH antagonist. The study will also compare patients undergoing elective fertility preservation versus PGT-A (pre-implantation genetic testing for aneuploidy) patients.The study will have a crossover design so that patients will receive both forms of treatment. The investigators will also compare the endocrine profile and ovarian response of CFA/PPOS versus rFSH/GnRH ovarian stimulation cycles.
This description comes directly from the study's public registry record.
Dominic Stoop, Prof. dr. · 093321699 · Dominic.Stoop@uzgent.be
Kathleen Wijnant, Msc · +32(0)93323013 · Kathleen.Wijnant@uzgent.be
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| University Hospital Ghent | Ghent, Belgium | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06175832