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The Role of the Physiological Endometrial Microbiota in Assisted Reproduction Outcomes

The Role of the Physiological Endometrial Microbiota in Assisted Reproduction Outcomes

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07606053
Acronym
no exist
Enrollment
80
Registered
2026-05-26
Start date
2025-01-02
Completion date
2026-06-25
Last updated
2026-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Microbiota, Repeated IVF Failure

Keywords

Physiological Endometrial Microbiota, Endometrial Microbiota, IVF, In vitro fertilization, Assisted reproduction, Implantation success, Embryo, Endometrial Microbiome, Microbiota, Microbiome

Brief summary

The goal of this observational study is to investigate the influence and contribution of the normal composition and balance of the endometrial microbiota on the achievement of embryo implantation and the maintenance of pregnancy in women undergoing IVF, with comparable clinical profiles, including patients with a history of RIF or RPL, evaluated under identical treatment protocols and hormonal conditions. The main questions it aims to answer are: 1. Does the normal composition of the endometrial microbiota, particularly the dominance of Lactobacillus species, influence embryo implantation success in women undergoing IVF? 2. Does the endometrial microbiota profile affect pregnancy maintenance, ongoing pregnancies, and live birth rates in women with a history of recurrent implantation failure (RIF) or recurrent pregnancy loss (RPL) Participants will not undergo any additional interventions beyond standard clinical care.They will provide clinical data already collected as part of routine IVF procedures.

Detailed description

Endometrial biopsies were collected from patients using a Pipelle catheter during the designated phase of the menstrual cycle. Each sample was immediately placed in a specialized preservative solution and transported to two external laboratories for analysis. In the first laboratory, bacterial DNA was extracted using a CE-IVD kit, followed by targeted amplification and barcoded sequencing of seven hypervariable regions (V2, V3, V4, V6, V7, V8, V9) of the 16S rRNA gene using the 16STM metagenomic kit and Ion Torrent sequencing system (Ion GeneStudio S5 with Ion Chef Instrument). Data were analyzed with Ion Reporter™ software and MicroSEC ID, using MicroSEC ID and Greengenes databases for taxonomic classification. In the second laboratory, total DNA was extracted, and targeted amplification of the 16S rRNA gene was performed using the 16S Barcoding Kit 24 V14 (Nanopore), followed by NGS on the MinION Mk1C analyzer. Bioinformatic analysis was conducted using the EPI2ME Labs 16S workflow. Bacterial composition was classified at the genus level, with results expressed as relative abundance percentages. OTU-level data were not disclosed. Interpretation of microbiota profiles was performed by the treating physician or clinical geneticist. Patients whose samples showed decreased Lactobacillus abundance or the presence of potentially pathogenic microorganisms received individualized interventions. These interventions included a two-week course of antibiotics tailored to the patient's clinical history, followed by probiotics administered orally or via combined oral and vaginal routes for two weeks to two months. Antifungal agents were administered when clinically indicated. Embryo transfer schedules were adapted based on microbial profiles and clinical assessment. Patients with normal microbial profiles proceeded with IVF in the next cycle. Patients with abnormal profiles, signs of inflammation, or potential pathogenic colonization had embryo transfer postponed for at least one month following completion of the therapeutic regimen. The study provides a detailed methodological framework for endometrial microbiota analysis, including sample collection, DNA extraction, sequencing strategies, bioinformatic pipelines, and clinical decision-making based on microbial composition, aiming to support personalized management in assisted reproduction.

Interventions

None listed

Sponsors

Assisting Nature
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 54 Years
Healthy volunteers
No

Inclusion criteria

1. Individuals who are biologically female. 2. Age between 18 and 54 years, in accordance with the legally permitted age limits for embryo transfer in Greece. 3. Undergoing in vitro fertilization (IVF) treatment. 4. Clinical history consistent with recurrent implantation failure (RIF) or recurrent pregnancy loss (RPL) and comparable IVF treatment profiles. 5. Ability to provide informed consent for the use of clinical and microbiome data for research purposes

Exclusion criteria

1. Individuals who are not biologically female. 2. Age below 18 or above 54 years. 3. Absence of endometrial biopsy samples or incomplete clinical data. 4. Presence of significant uterine abnormalities or medical conditions that contraindicate embryo transfer. 5. Participation in another interventional clinical study that may interfere with microbiome assessment or IVF outcomes.

Design outcomes

Primary

MeasureTime frameDescription
Implantation Rate according to microbiome profileFrom the day of the embryo transfer to the day of confirmation of implantation (2-4 weeks)The study formally assesses differences in embryo implantation rates between women with Lactobacillus-dominant and non-Lactobacillus-dominant endometrial microbiota profiles.
Ongoing Pregnancy/Live Birth Rate according to microbiome profileFrom the day of embryo transfer up to the end of the first trimester (up to 12 weeks of gestation) and live birth until delivery (up to 40 weeks of gestation)Association between endometrial microbiota composition and the likelihood of achieving an ongoing pregnancy or live birth
Biochemical pregnancy rate and microbiome statusFrom the day of embryo transfer to the day of confirmation of implantation (2-4 weeks)Rate of biochemical pregnancies in relation to endometrial microbiota profile

Secondary

MeasureTime frameDescription
Endometrial microbiota compositionAt time of biopsy collection (during procedure)Relative abundance of Lactobacillus versus non-Lactobacillus genera in endometrial biopsies analyzed by 16S rRNA sequencing.

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 27, 2026