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Clinical Trials/NCT02009891
NCT02009891CompletedNot Applicable

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

Ottawa Fertility Centre1 site in 1 country200 target enrollmentStarted: June 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
Clinical pregnancy rate at 8 -10 weeks gestational age

Study Overview

Brief Summary

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).

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 38 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

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 -

Outcomes

Primary Outcomes

Clinical pregnancy rate at 8 -10 weeks gestational age

Time Frame: 36 months

Secondary Outcomes

  • Multiple pregnancy rate(36 months)

Investigators

Sponsor
Ottawa Fertility Centre
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Arthur Leader

Consultant

Ottawa Fertility Centre

Study Sites (1)

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