Impact of a Predetermined Day 5 ET vs. a Predetermined Day 6 ET on Clinical Pregnancy Rate After ICSI Treatment

Recruiting Observational Study
Infertility Reproductive Issues
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Female
Study type
Observational
Participants needed
2,400 (estimated)
Sponsor
Infertility Treatment Center Dortmund · Other
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About This Trial
The aim of this prospective multicenter study is to investigate the influence of a predetermined embryo transfer on day 6 compared to a predetermined embryo transfer on day 5. The study population consists of the control group (predetermined embryo transfer on day 5) and the study group (predetermined embryo transfer on day 6). The primary endpoint is the clinical pregnancy rate (detection of a ge…
Trial Locations
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Eligibility Criteria
Inclusion criteria: The patients to be included should be ≥18 years old. There is no upper age limit. Only ICSI treatments with a single embryo transfer (SET) should be included. Only the first cycle per patient should be evaluated. Exclusion criteria: none
Contacts

Stefan Dieterle, MD

00492315575450

dieterle@kinderwunschzentrum.org

CONTACT

Tom Trapphoff, DR

00492315575450

trapphoff@kinderwunschzentrum.org

CONTACT