Actively Recruiting
Impact of a Predetermined Day 5 Versus Day 6 Embryo Transfer on Clinical Pregnancy Rate After ICSI Treatment
Led by Infertility Treatment Center Dortmund · Updated on 2025-07-24
2400
Participants Needed
1
Research Sites
8 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
This research aims to compare the effects of transferring embryos on day 5 versus day 6 after intracytoplasmic sperm injection (ICSI) treatment in women facing infertility or reproductive issues. The study is prospective and multicenter, including participants from three fertility centers. It investigates whether delaying embryo transfer to day 6 influences the clinical pregnancy rate and abortion rate, as no prior prospective studies have directly compared these two specific timing options. Participants are divided into two groups: a control group receiving embryo transfers on day 5 and a study group receiving transfers on day 6. The control group includes patients with oocyte pick-up on various days leading to day 5 transfers, while the study group includes patients with oocyte pick-up on a specific day leading to day 6 transfer. This design allows comparison of the clinical outcomes between predetermined embryo transfers on day 5 and day 6 after ICSI. During the study, clinical pregnancy is assessed by detecting a gestational sac four weeks after embryo transfer, which is the primary outcome. The abortion rate per clinical pregnancy is monitored throughout the ongoing pregnancy as a secondary outcome. Data collection takes place at multiple fertility centers, and the study includes only women aged 18 or older undergoing their first ICSI cycle with a single embryo transfer. Participants are observed through the pregnancy period to evaluate these outcomes.
CONDITIONS
Brief 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 aged 18 years or older
- Only women undergoing intracytoplasmic sperm injection (ICSI) treatment
- Single embryo transfer (SET) during treatment
- Only the first ICSI treatment cycle per patient is included
You will not qualify if you...
- None reported for this study population and design
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 4 weeks after embryo transfer
Participants undergo embryo transfer on a predetermined day (either day 5 or day 6) following intracytoplasmic sperm injection (ICSI) treatment and are monitored for clinical pregnancy outcomes.
1 visit for embryo transfer and follow-up visits within 4 weeks
Duration - During entire ongoing pregnancy
Participants who achieve clinical pregnancy are monitored throughout the ongoing pregnancy to assess abortion rates.
Regular follow-up visits during pregnancy
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
T
Tom Trapphoff, DR
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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