About this trial

To evaluate, in a randomized controlled trial, whether AI-guided monitoring and ovulation triggering leads to clinical outcomes comparable to those achieved through physician-led decision-making in patients undergoing ovarian stimulation for IVF.

Eligibility criteria

Qualifiers

Undergoing COS for IVF with autologous oocytes, oocyte donation and elective fertility preservation with all monitoring USS (ultrasound scan) conducted at our centers.

Disqualifiers

Medically indicated fertility preservation

Inability to attend clinic visits for monitoring.

Trial design

Treatments tested in this trial

  • STIMAI®.
  • Routine clinical management

Treatment groups

644 Participants
are divided into 2 treatment groups

Locations

5
Dexeus Mujer Sabadell SabadellBarcelona, Spain
Dexeus Mujer Sant Cugat08195, Sant Cugat del VallèsBarcelona, Spain
Dexeus Mujer Reus43202, ReusTarragona, Spain
Hospital Universitario Quiron Dexeus08028, Barcelona Spain

Sponsors and collaborators

Fundacion Dexeus

Lead sponsor