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Completed No phase listed Observational

Evaluation of the Efficacy of Diafert in Predicting Embryos' Potential to Develop to the Blastocyst Stage

ClinicalTrials.gov ID: NCT02788617

Public ClinicalTrials.gov record NCT02788617. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 12, 2026, 12:02 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Non-interventional, Multicenter, Clinical Study to Evaluate the Efficacy of the Diafert G-CSF ELISA as an Adjunct to Morphological Assessment in Predicting Embryos' Potential to Develop to the Blastocyst Stage

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This prospective study will evaluate the efficacy of Diafert as an adjunct to morphological assessment in predicting embryos' potential to develop to the blastocyst stage on Day 5.

Study identification

NCT ID
NCT02788617
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Forest Laboratories
Industry
Enrollment
100 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 23, 2016
Primary completion
Jan 29, 2017
Completion
Apr 3, 2017
Last update posted
Jul 30, 2017

2016 – 2017

United States locations

U.S. sites
9
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
Huntington Reproductive Center Encino California 91436
Women's Medical Research Group Clearwater Florida 33759
InVia Fertility Specialists Hoffman Estates Illinois 60169
Institute for Reproductive Health Cincinnati Ohio 45209
Main Line Fertility Center Bryn Mawr Pennsylvania 19010
Dallas - Fort Worth Fertility Associates Dallas Texas 75231
Houston Fertility Institute Houston Texas 77063
Utah Fertiity Center Pleasant Grove Utah 84062
Reproductive Care Center Sandy City Utah 84092

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02788617, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 30, 2017 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02788617 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →