A Prospective Study to Evaluate the Outcome of the Aurora Test Used With Blastocyst Transfer in an ICSI Cycle (Aurora-Blasto)

Recruiting N/A Interventional Study
Infertility Assisted Reproductive Technology
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 40
Sex
Female
Study type
Interventional
Purpose
Supportive Care
Participants needed
1,028 (estimated)
Sponsor
University Hospital, Ghent · Other
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About This Trial
In current treatments for In Vitro Fertilization (IVF) and Intracytoplasmic Sperm Injection (ICSI), the creation of multiple embryos is a common practice. The decision to transfer an embryo is traditionally based on the morphological assessment by an embryologist, which, due to its nature, must be considered subjective. In certain regions, invasive embryo biopsy techniques, such as Preimplantation…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patients undergoing ICSI treatment, with maximum 40 years of age at time of signing the ICF 2. Patients stimulated with GnRH antagonist/HP-hMG or GnRH antagonist/recFSH, scheduled for fresh SET Day 5 with hCG or dual trigger (hCG + GnRH agonist) or Patients stimulated with Gn…
Contacts

Dominic Stoop

003293321699

Dominic.Stoop@uzgent.be

CONTACT