Image

Aurora Test for ART Donor Patients (AURORA-Donor)

Aurora Test for ART Donor Patients (AURORA-Donor)

Recruiting
18-35 years
Female
Phase N/A

Powered by AI

Overview

This is a randomized observational study. The main aim is to determine potential oocyte competence predictive mRNA expression profiles in the cumulus cells isolated form individual oocytes. In 2 patient cohorts: 1)GnRH Antagonist & hr-FSH with GnRH Agonist trigger, 2) Progesterone & hr-FSH with GnRH Agonist trigger.

Eligibility

Inclusion Criteria Donor:

  • Patients are 18 to 35 years old
  • BMI between 17-30
  • Regular menstrual cycles
  • AFC > 8
  • Patient profile in compliance with SEF (Sociedad EspaƱola de Fertilidad) directives for egg donation (medical, psychological and genetic screening, informed consent)
  • Patients' stimulation: GnRH Antagonist & hr-FSH with GnRH Agonist trigger or Progesterone & hr-FSH with GnRH Agonist trigger
  • Patients agree that the oocytes will be denuded for cumulus testing and provide written informed consent for participation to the study

Exclusion Criteria Donor:

  • BMI < 17 or > 30
  • Extreme irregular menstrual cycles (<20 days or >40 days)
  • AFC < 8
  • <8 MII on previous egg retrieval
  • Women with history of poor oocyte maturation or known maturation defect or unexplained failure in previous treatments
  • Patients that fail to comply with SEF (Sociedad EspaƱola de Fertilidad) directives for egg donation (medical, psychological and genetic screening, informed consent)

Inclusion Criteria Recipient:

  • Patients applying for ART egg donation with fresh/frozen sperm from the partner or frozen donor sperm. With eSB-FET in modified natural cycle or an HRT cycle.
  • Patients are from 18 to 50 years old.
  • Patients will be treated by ICSI (intracytoplasmic sperm injection) and eSB-FET (elective Single Blastocyst Frozen Embryo Transfer)
  • Recipient patients agree that the donors' oocytes will be denuded for cumulus testing and provide written informed consent for participation to the study

Exclusion Criteria for oocyte Recipients

  • Patient included in any other prospective study.
  • BMI < 17 or > 35
  • Severe uterine factor: Multiple myomectomy, multiple fibroids, major uterine malformation (unicorn, septum), Asherman Sd, severe adenomyosis
  • Repeated Implantation Failure or Repeated Pregnancy Loss after euploid Single Blastocyst Transfer
  • Severe male factor: Abnormal Caryotype or FISH, severe OAT / Cripto-Azoospermia, DNA Fragmentation >50% after medical treatment
  • TESE / TESA (testicular sperm extraction/aspiration)

Study details
    Infertility

NCT06280677

Fertiga, Belgium

16 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.