Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
All Genders
Healthy Volunteers
NCT04255615

Use of Artificial Intelligence for Clinical Assessment of Assisted Reproductive Techniques and IVF Outcomes

Led by Weill Medical College of Cornell University · Updated on 2025-12-24

4000

Participants Needed

1

Research Sites

502 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The use of machine learning techniques using an artificial intelligence tool is proposed to analyze clinical data to predict best possible IVF/ART outcomes. This tool has been utilized to accurately predict embryo quality here at Cornell. Utilizing this tool to assess objective clinical findings and predict outcomes of assisted reproductive techniques is sought, with the ultimate goal of an automated tool to reduce implicit physician bias. Within this goal, using this tool to objectively and accurately assess baseline ovarian reserve at the start of an ART cycle is proposed, using 3D sonography to image the ovary and artificial intelligence tool to objectively identify baseline antral follicle counts.

CONDITIONS

Official Title

Use of Artificial Intelligence for Clinical Assessment of Assisted Reproductive Techniques and IVF Outcomes

Who Can Participate

Age: 18Years - 89Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing ovarian stimulation including ovulation induction and IVF cycles
  • Treatment includes fresh embryo transfer and cryopreservation of oocytes or embryos
  • Healthy male partners of female participants who agree to join the study
Not Eligible

You will not qualify if you...

  • None

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Weill Cornell Medicine

New York, New York, United States, 10021

Actively Recruiting

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Research Team

N

Nikica Zaninovic, PhD

CONTACT

R

Rodriq Stubbs, NP

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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