The Embryo-endometrium Multifaceted Interface: Endometrial Cavity Molecular Microbiobial and Transcriptomic Signatures in Predictinf Pregnancy Outcome in Infertile Patients Undergoing Assisted Reproduction Technology Procedures
1 other identifier
observational
322
1 country
1
Brief Summary
In reproductive medicine, a fundamental challenge is to evaluate the endometrial health status during the embryo implantation window as a limiting step in predicting the success of treatments of assisted reproduction technology (ART). Some highthroughput tools, recently developed by private genomics companies, are available in the market even if they have not been independently validated and have different limitations. We propose a prospective cohort study with the aim of validating the reliability and increasing efficacy of these tools. Endometrial fluid samples will be collected non-invasively from women undergoing ART cycles and isolated genetic materials will be subjected to 16S rRNA gene sequencing for microbiota profiling and to RNAseq analysis of RNA content of extracellular vesicles previously recognized as a tissue proxy in predicting endometrial receptivity. Clinical pregnancy rate/first cycle will be the target outcome used to assess the resulting predictive models. Ultrasonographic features of the endometrium will also be collected and accounted for in the predictive model.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 24, 2021
CompletedFirst Submitted
Initial submission to the registry
June 13, 2025
CompletedFirst Posted
Study publicly available on registry
July 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2025
CompletedJuly 25, 2025
July 1, 2025
4.8 years
June 13, 2025
July 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Identification of endometrial microbiome diversity
Evaluation of the endometrial microbiome composition and diversity using 16S rRNA sequencing to assess the functional impact of the endometrial microbial community in predicting the clinical pregnancy rate in women undergoing ART cycles.
through study completion, an average of 1 year
Extracellular Vesicle (EV) RNA Profiles
Quantification of extracellular vesicle (EV) RNA expression profiles from uterine fluid samples using RNA sequencing (expressed in CPM). Confirmation of the good correlation between expression of genes in tissue samples and in endometrial-derived EVs.
through study completion, an average of 1 year
Integrated Predictive Model for Clinical Pregnancy
Development of a multivariable predictive model combining endometrial microbiome diversity, EV RNA profiles, and ultrasound-AI analysis to predict clinical pregnancy rates in ART cycles.
through study completion, an average of 1 year
Study Arms (2)
fertile women
Reference group
infertile women undergoing ART cycles
Cases group
Eligibility Criteria
The study population is composed of women undergoing assisted reproduction treatments, specifically in vitro fertilization (IVF). These patients are followed in an outpatient setting at two specialized infertility centers in Italy: San Raffaele Hospital and Fondazione Cà Granda Policlinico. They are women who have been referred to IVF due to infertility, and are starting their first IVF cycle. All participants meet specific inclusion criteria, such as being between 18 and 39 years of age, having normal uterine anatomy, and no evidence of hydrosalpinx on ultrasound examination. The outpatient nature of the study allows for non-invasive sampling procedures and routine follow-up without the need for hospitalization. This setting reflects real-world clinical practice in reproductive medicine, ensuring that the findings will be directly applicable to standard IVF care. Additionally, the study includes a group of fertile women, also managed on an outpatient basis, who serve as a reference.
You may qualify if:
- Indication to ART
- Age 18-39 years
- First ART cycle
- Normal uterine morphology and no hydrosalpinx at ultrasound
You may not qualify if:
- Poor responders according to Bologna criteria
- Indications to ART for severe male infertility
- Subjects will be cycling women with proven fertility undergoing laparoscopy for tubal ligation
- BMI \< 30
- Aged 20 to 40 years
- Smokers
- Not taking any medication
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
OSR Innate Immunity and tissue remodeling Unit and Centro Scienze Natalità OS
Milan, milano, 20133, Italy
Biospecimen
Uterine fluid samples
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD, PhD
Study Record Dates
First Submitted
June 13, 2025
First Posted
July 25, 2025
Study Start
January 24, 2021
Primary Completion
October 31, 2025
Study Completion
November 30, 2025
Last Updated
July 25, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share