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OpenTrials
Completed

NCT Number: NCT02009891

Use of Predictive Model to Assist Patients Having an Embryo Transfer After IVF

To determine in women undergoing IVF who are at high risk of multiple births (>35%), as calculated by the application of a predictive model - IVFsingleTM, if single embryo transfer will lead to both comparable clinical pregnancy rate (CPR) and other secondary outcomes such as live birth rate (LBR) and cumulative live birth rate (cLBR) in comparison to DET while reducing the incidence of multiple births (a secondary outcome measure).

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Key information

Age range

18 year–38 year

Sex eligibility

Female

Study type

Observational

Primary location

Ottawa Fertility Centre

Ottawa, Ontario, K2C3V4, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Under 38 1st or second IVF attempt

-

Exclusion criteria

Over 37 years old donor egg third or greater IVF attempt cancellation in previous cycle for poor response successful pregnancy with IVF -

Treatment and study plan

Primary outcomes

  1. Clinical pregnancy rate at 8 -10 weeks gestational age

    Time frame: 36 months

Secondary outcomes

  1. Multiple pregnancy rate

    Time frame: 36 months

Sponsors and collaborators

Lead sponsor

Ottawa Fertility Centre

Other

Registry information

Official study title

The Application of a Validated Patient and Clinic Specific Predictive Model to Reduce the Incidence of Multiple Births Resulting From Fresh In Vitro Fertilization Cycles

Important dates

Study start
2012
Primary completion
2016
Study completion
2016
First posted
Dec 12, 2013
Registry last updated
Sep 25, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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