Clinical Cohort Study on the Endocrinology and Vaginal/Endometrial Microbiome of the Luteal Phase in Assisted Reproduction

ConditionInfertility
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorUniversity of Luebeck

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 18 to 45 years

Transfer of cryopreserved embryos

Disqualifiers

Fresh IVF/ICSI embryo transfer cycle

Evidence for ovulation on ultrasound previous to embryo transfer confirmed by a follicle ≥14mm or by a progesterone ≥1.0 µg/l in programmed cycles

Uterus malformations, endometrial abnormalities (on ultrasound or diagnosed by previous hysteroscopy)

Trial population

Patients attending infertility clinic.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Blood samples and microbiological swaps

    Diagnostic test

    Blood analysis and analysis of vaginal microbiota.

Treatment groups

1,200 Participants
are divided into 4 treatment groups
Group A: Progynova/Dydrogesterone1 intervention
Group B: Spontaneous cycle1 intervention
Group C: Progynova/Crinone1 intervention
Group D: Others Medication1 intervention

Trial outcomes

Primary outcomes

1

Serum progesterone (microgram/Liter) levels.

Time frame
31.12. 2020

Secondary outcomes

1

Change of vaginal microbiome between follicular phase, luteal phase and early pregnancy

Time frame
31.12.2022
2

Vaginal bleeding pattern in the luteal phase and early pregnancy in frozen-thawed embryo transfer cycles

Time frame
31.12.2022
3

Association of endocrine values and bleeding, microbiome status and treatment outcome

Time frame
31.12.2022

Other outcomes

Sponsors and contacts

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