Actively Recruiting
Clinical Cohort Study on the Endocrinology and Vaginal/Endometrial Microbiome of the Luteal Phase in Assisted Reproduction
Led by University of Luebeck · Updated on 2025-05-22
1200
Participants Needed
5
Research Sites
530 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Rationale: The hormone progesterone has different functions. In pregnancy, it is vital for maintenance thereof. In early pregnancy, progesterone is synthesized by the Corpus luteum (CL). Its production shifts from the CL to the placenta after several gestational weeks. This process is termed luteoplacental shift. Still, the exact time point of the luteoplacental shift remains unknown. Furthermore, the characteristics of placental progesterone increase and its relevance for the course of pregnancy has not been studied so far. Furthermore, recent studies have shown an influence of abnormal vaginal microbiota on the likelihood to achieve and maintain pregnancy. Little is known about possible crosslinks between endocrinology and vaginal/endometrial microbiota which is why this study aims to investigate possible associations of such kind. Objective: The primary objective of this study is to evaluate the time point of the luteoplacental shift in patients achieving pregnancy after transfer of cryopreserved embryos subsequently to IVF/ICSI cycles. Secondary objectives are to study the characteristics of the placental progesterone increase and its function as a predictor of the course and development of pregnancies and to study vaginal/endometrial microbiota at baseline and changes associated with shift into luteal phase and early pregnancy and how this potentially relates to pregnancy outcome. Study Design: Prospective, multi-center, observational clinical cohort study. For the primary objective, data from a single center will be also be retrospectively analyzed. Study population: Female patients aged 18 to 45 years undergoing transfer of embryos after freezing and thawing 2PN oocytes or embryos. Interventions: Blood withdrawal, vaginal/endometrial swabs and endocrine and microbiom analyses. Study parameters/endpoints: The main parameter is time point of progesterone increase in pregnancy in relation to initial progesterone levels by pregnancy status. Secondary, slope and magnitude of placental progesterone increase and its relevance as a predictor for the course and development of pregnancies/babies. Furthermore, vaginal microbiota of women undergoing embryo transfer and of women in early pregnancy are parameter of this study.
CONDITIONS
Official Title
Clinical Cohort Study on the Endocrinology and Vaginal/Endometrial Microbiome of the Luteal Phase in Assisted Reproduction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 45 years
- Transfer of cryopreserved embryos
You will not qualify if you...
- Fresh IVF/ICSI embryo transfer cycle
- Evidence of ovulation before embryo transfer confirmed by ultrasound follicle 6mm or progesterone 1.0 bcg/L in programmed cycles
- Uterus malformations or endometrial abnormalities diagnosed by ultrasound or previous hysteroscopy
AI-Screening
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Trial Site Locations
Total: 5 locations
1
IVF-SAAR
Saarbrücken, Saarland, Germany, 66113
Actively Recruiting
2
Universitäres Kinderwunschzentrum Lübeck
Lübeck, Schleswig-Holstein, Germany, 23562
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3
Universitätsklinikum Düsseldorf,UniKiD
Düsseldorf, Germany, 40225
Actively Recruiting
4
Universitäres Kinderwunschzentrum
Kiel, Germany, 24105
Actively Recruiting
5
University of Luebeck
Lübeck, Germany
Actively Recruiting
Research Team
G
Georg Griesinger, MD
CONTACT
T
Tanja Eggersmann, MD
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
4
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