Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
ID07110285

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.

Led by FertilAI · Updated on 2026-01-12

180

Participants Needed

1

Research Sites

55 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on patients undergoing ovarian stimulation cycles using the GnRH antagonist protocol for either oocyte cryopreservation or fertilization via intracytoplasmic sperm injection (ICSI). It aims to compare the number of mature eggs produced when the timing of the trigger day is decided by physicians versus an artificial intelligence-based algorithm. The study evaluates how these two approaches affect in-vitro fertilization (IVF) outcomes. Participants are randomly assigned to one of two groups: one where the trigger day timing is determined by the treating physician, and another where an artificial intelligence-based algorithm makes this decision. This intervention occurs during the ovarian stimulation cycle involving GnRH antagonist protocols, with mature oocyte yield as the primary measure. Throughout the study, researchers will monitor the number of mature eggs collected over a two-year period. Participants will undergo standard ovarian stimulation and oocyte retrieval procedures, with outcomes measured by mature and total oocyte yield. The study includes follow-up to assess these outcomes and ensure patient safety during the trial period, which spans from May 2025 to May 2028.

CONDITIONS

Brief Title

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.

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing an ovarian stimulation cycle using the GnRH antagonist protocol for oocyte cryopreservation or fertilization via intracytoplasmic sperm injection (ICSI)
  • Age between 18 and 45 years
Not Eligible

You will not qualify if you...

  • Loss to follow-up
  • Patient retracts consent to participate

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Duration of one ovarian stimulation cycle

Participants undergo ovarian stimulation using the GnRH antagonist protocol, with trigger day timing decided either by their physician or by an artificial intelligence-based algorithm.

1 baseline visit and several monitoring visits during stimulation

Trial Site Locations

Total: 1 location

1

Herzliya Medical Center

Herzliya, Israel, 74077

Actively Recruiting

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Research Team

M

Michal Youngster, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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