Follow-up protocol to collect the outcome of frozen-thawed embryo transfer cycles after cryopreservation of embryos in clinical trial 107012
- Conditions
- Controlled Ovarian Stimulation (COS) to induce the development of multiple follicles in patients participating in an Assisted Reproductive Technology (ART) program
- Registration Number
- EUCTR2006-003813-42-SE
- Lead Sponsor
- V Organon
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
1. Subjects from whom embryos have been cryopreserved in Trial 107012 of which at least
one embryo is thawed for use in a subsequent FTET cycle;
2. Able and willing to give written informed consent.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
None.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: To collect the outcome of frozen-thawed embryo transfer cycles after the embryos are cryopreserved in Trial 107012, in order to estimate the cumulative pregnancy rate for each treatment group.;Secondary Objective: ;Primary end point(s): Cumulative ongoing pregnancy rate; the cumulative ongoing pregnancy rate is the percentage of subjects who started controlled ovarian stimulation treatment in Trial 107012 and have an ongoing pregnancy either immediately after embryo transfer in Trial 107012 or after one or more frozen-thawed embryo transfer cycles following cryopreservation.
- Secondary Outcome Measures
Name Time Method