Herzliya Medical Center
Herzliya, 74077, Israel
Location status: Recruiting
Location contact
Ariel Hourvitz, MD
SUB_INVESTIGATOR
Michal Youngster
CONTACT
Michal Youngster, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07110285
To compare the number of mature oocytes following a GnRH antagonist in-vitro fertilization stimulation cycle when comparing trigger day timing decision by physicians versus an artificial intelligence-based algorithm
Interested in participating?
Request Info18 year–45 year
All sexes
Interventional
Not applicable
Herzliya, 74077, Israel
Location status: Recruiting
Ariel Hourvitz, MD
SUB_INVESTIGATOR
Michal Youngster
CONTACT
Michal Youngster, MD
PRINCIPAL_INVESTIGATOR
Examination of all patients undergoing an ovarian stimulation cycle utilizing the GnRH antagonist protocol for oocyte cryopreservation or for fertilization via intracytoplasmic sperm injection (ICSI) (any treatment where oocytes are denuded and maturity may be assessed). The number of mature oocytes will be compared between cycles where trigger day timing was decided by the treating physician versus an artificial intelligence-based algorithm.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Trigger day timing decision by an artificial intelligence-based algorithm
Time frame: 2 years
The number of mature oocytes collected during a single egg retrieval cycle
Time frame: 2 years
Number of retrieved oocytes during an egg collection cycle
Contact information is provided by the study sponsor or research team.
FertilAI
Industry
Ovarian Stimulation Outcomes During a GnRH Antagonist Protocol for In-vitro Fertilization When Comparing Trigger Day Decision by Physicians Versus an Artificial Intelligence-based Algorithm - A Randomized Control Study.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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