Actively Recruiting
Impact of a Predetermined Day 5 ET vs. a Predetermined Day 6 ET on Clinical Pregnancy Rate After ICSI Treatment
Led by Infertility Treatment Center Dortmund · Updated on 2025-07-24
2400
Participants Needed
1
Research Sites
192 weeks
Total Duration
On this page
Sponsors
I
Infertility Treatment Center Dortmund
Lead Sponsor
F
Fertility Center Dortmund
Collaborating Sponsor
AI-Summary
What this Trial Is About
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 gestational sac) per embryo transfer and the secondary endpoint is the abortion rate per clinical pregnancy. The data from the multicenter study are obtained at three test centers (Fertility Center Dortmund, Fertility Center Essen and Fertility Center Bad Münder).
CONDITIONS
Official Title
Impact of a Predetermined Day 5 ET vs. a Predetermined Day 6 ET on Clinical Pregnancy Rate After ICSI Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients must be 18 years or older
- Only patients undergoing ICSI treatments with a single embryo transfer (SET) are included
- Only the first ICSI treatment cycle per patient is considered
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Infertility treatment center Dortmund
Dortmund, North Rhine-Westphalia, Germany, 44135
Actively Recruiting
Research Team
S
Stefan Dieterle, MD
CONTACT
T
Tom Trapphoff, DR
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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