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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02009891
Other study ID # 100OFC
Secondary ID
Status Completed
Phase N/A
First received December 9, 2013
Last updated September 21, 2017
Start date June 2012
Est. completion date October 2016

Study information

Verified date September 2017
Source Ottawa Fertility Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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).


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 38 Years
Eligibility 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 -

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Canada Ottawa Fertility Centre Ottawa Ontario

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Fertility Centre

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical pregnancy rate at 8 -10 weeks gestational age 36 months
Secondary Multiple pregnancy rate 36 months
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