Actively Recruiting
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
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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
Eligibility Criteria
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
You will not qualify if you...
- Loss to follow-up
- Patient retracts consent to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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