CClinicalTrials.gg
Status unknownNCT01816802MERGEUpdated Mar 26, 2015

Registry Study of Traditional Morphology Grading Combined With Eeva in IVF Treatment

An observational study in Infertility, sponsored by Progyny, Inc.. Status unknown at 12 sites in United States. Open to female participants. Per ClinicalTrials.gov, last updated 2015-03-26.

Sponsored by Progyny, Inc. · Observational

The sponsor has not verified this record recently (last verified Mar 2015), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,200
Sex
Female
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Study summary

The purpose of this study is to record and evaluate the use of traditional morphology grading combined with Eeva in the treatment of in vitro fertilization.

Read the detailed description

This is a prospective, observational, single-arm, nonrandomized, multicenter study. Data will be collected to establish eligibility, at baseline, during the stimulation and in vitro fertilization process, during embryo culture, at embryo transfer, at 12-18 days post egg retrieval to verify biochemical pregnancy, and then typically at 5-6 weeks gestational weeks to verify clinical pregnancy.

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Conditions studied

  • Infertility

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Keywords

  • In vitro fertilization
  • Assisted reproductive therapy
  • Time-lapse image recording
  • Image analysis software
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In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's planned enrollment of 1,200 is above the median of 200 across 714 observational studies indexed under Infertility.

Browse Infertility studies →

Lead sponsor

Progyny, Inc. is the lead sponsor of 10 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients undergoing in vitro fertilization treatment who provide informed consent and use Eeva in their treatment cycle.

Inclusion criteria

  • women undergoing fresh in vitro fertilization treatment using their own eggs or donor eggs.

Exclusion criteria

Exclusion Criteria:

  • history of cancer.
  • gestational carrier.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,200 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes

Groups and cohorts

  • In-vitro fertilization using Eeva

    Patients undergoing in-vitro fertilization treatment who provide informed consent and use Eeva in their treatment cycle.

    Device: In-vitro fertilization using Eeva

Interventions

  • DeviceIn-vitro fertilization using Eeva

    Eeva will image embryos through cleavage stage (Day 3). Embryologists will use Eeva results along with traditional morphological grading to assist in selecting embryo(s) for transfer or freezing.

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What researchers measure

Primary outcomes

  1. Clinical Pregnancy Rate

    Determined by first pregnancy ultrasound outcome and optional 12-month phone follow-up

    Time frame: 5-6 gestational weeks

Other outcomes

  1. Multiple Pregnancy Rate

    Determined by follow-up pregnancy ultrasound outcome

    Time frame: 5-6 gestational weeks

  2. Spontaneous Miscarriage Rate

    Determined by follow-up pregnancy ultrasound outcome

    Time frame: 5-6 gestational weeks

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Study locations

12 sites
  • HRC Fertility
    Encino, California 91436, United States
  • Stanford Fertility and Reproductive Medicine Center
    Palo Alto, California 94304, United States
  • Reproductive Partners
    Redondo Beach, California 90277, United States
  • Pacific Fertility Center
    San Francisco, California 95124, United States
  • Center for Advanced Reproductive Services (UCHC)
    Farmington, Connecticut 06030, United States
  • Fertility Centers of Illinois - River North
    Chicago, Illinois 60610, United States
  • Northwestern Medical Faculty Foundation
    Chicago, Illinois 60611, United States
  • Fertility Centers of Illinois, Highland Park IVF Center
    Highland Park, Illinois 60035, United States
  • Long Island IVF
    Melville, New York 11747, United States
  • University Hospital Fertility Center
    Beachwood, Ohio 44122, United States
  • Institute for Reproductive Health
    Cincinnati, Ohio 45209, United States
  • Fertility Center of San Antonio
    San Antonio, Texas 78229, United States
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 26, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01816802
Lead sponsor
Progyny, Inc.
Responsible party
Sponsor
First posted
Mar 22, 2013
Start date
Feb 2013
Primary completion
Jun 2015 (estimated)
Completion
Jun 2015 (estimated)
Last update
Mar 26, 2015

Study contacts

Shehua Shen, MD
study director · Progyny, Inc.

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

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