NCT07085585

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

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
322

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2021

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 24, 2021

Completed
4.4 years until next milestone

First Submitted

Initial submission to the registry

June 13, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 25, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2025

Completed
Last Updated

July 25, 2025

Status Verified

July 1, 2025

Enrollment Period

4.8 years

First QC Date

June 13, 2025

Last Update Submit

July 24, 2025

Conditions

Keywords

Extracellular Vesiclesendometrial microbiomeRNA-Seq

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

Age18 Years - 40 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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

Location

Biospecimen

Retention: SAMPLES WITH DNA

Uterine fluid samples

MeSH Terms

Conditions

Infertility

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

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

Locations