Combined Use of Machine Learning and Metabolomics to Improve the Diagnosis and Management of Hyperandrogenism

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age16-45
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Hyperandrogenism is a common reason for consultation, the causes of which can range from common conditions (PCOS) to rarer conditions with major genetic implications (NC21OHD). It is characterized by elevated levels of circulating androgens, mainly testosterone. This excess of androgens usually manifests clinically as increased male-pattern hair growth and, less specifically, acne and alopecia. Its prevalence is estimated at between 6 and 12% in women of reproductive age, and its incidence is increasing.

It is also responsible for infertility. As a reminder, infertility is a major public health issue and affects more and more couples around the world.

The investigators therefore wish to develop innovative tools to improve the diagnosis and management of hyperandrogenism

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients of childbearing age (16 to 45 years old)

Suffering from hyperandrogenism

Established etiological diagnosis with elimination of differential diagnoses

Informed and not opposed to the collection of their data for the purposes of the study

Disqualifiers

Pregnancy

Patients under legal protection measures

Trial population

The first stage of the study will involve participating centers selecting patients' medical records after verifying their eligibility. It should be noted that the control group will consist of a population for whom tests were carried out for symptoms that were ultimately ruled out with normal results.

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

  • data collection

    Other intervention

    collection of data from medical records over a period of 5 years

Treatment groups

800 Participants
are divided into 1 treatment group
Group A: principal group1 intervention

Trial outcomes

Primary outcomes

1

Use of machine learning models combined with metabolomics to distinguish between different causes of hyperandrogenism

Time frame
5 years

Secondary outcomes

1

Use of metabolomics to improve the management of patients with hyperandrogenism

Time frame
5 years
2

Use of metabolomics to predict CYP21A2 genotyping results

Time frame
5 years
3

Study of the impact of anti-androgenic hormone therapy on the predictive capabilities of the model

Time frame
5 years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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