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Recruiting Observational

Assessment of the Effectiveness of the Metabolomic Approach in Screening for Endometrial Cancer

NCT06893861 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2023-07-06
Last updated
2025-03-25

Condition(s) studied

Endometrial Carcinoma (EC)

Investigational drug(s) / intervention(s)

Metabolomic profiling

Metabolomic profiling: Blood samples will be collected from these subjects, and following metabolomic profiling, the data will provide the foundation for training machine learning models capable of recognizing the metabolomic profiles of subjects with endometrial carcinoma and differentiating them from subjects with other conditions.

Study summary

The study involves the use of reagents or materials for diagnostic assessments that are not commercially available, specifically a metabolomic signature for screening endometrial carcinoma and/or other types of cancers, and follows a case-control design.

This study aims to achieve several objectives that contribute to evaluating the diagnostic potential of a specific "metabolomic signature" to be used for screening endometrial carcinoma. Specifically, the study seeks to assess the signature's discriminative ability in differentiating between benign endometrial neoplasms and neoplasms of different histological origins.

Eligibility

Sex
FEMALE
Min age
50 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Female sex 2. Age between 50 and 80 years 3. Willingness to participate in the study and signing of the informed consent 4. Clinical condition of post-menopause Exclusion Criteria: 1. Previous hysterectomy 2. Hormone replacement therapy 3. Immunosuppressive therapy

Primary outcome measure(s)

  • Creation and Testing of a Metabolomic Signature for Endometrial Carcinoma Screening — 24 months
  • Evaluation of the Ability of the Metabolomic Signature to Discriminate Between Neoplasms of Different Histological Origins — 24 months
  • Validation of the Developed Model in a Real-World Clinical Setting — 24 months

Trial sites (1)

FacilityCityRegionStatus
Istituto Nazionale Tumori | "Fondazione Pascale" Naples Italy Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06893861 on ClinicalTrials.gov ↗ ← All trials in Italy