Observational Study on the Causal Architecture of Polycystic Ovary Syndrome (PCOS)

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorAnnieGuard Corp.

About this trial

The goal of this observational study is to learn about the causal architecture of Polycystic Ovary Syndrome (PCOS) in women aged 18 to 45. The main questions it aims to answer are:

What does the hormonal, metabolic, and clinical architecture of PCOS look like across a diverse global population? Can the causal architecture of PCOS be reconstructed from existing lab results and clinical data? Are there distinct architectural patterns across different groups of women with PCOS? Participants who have been diagnosed with PCOS by a healthcare provider will complete an online questionnaire about their diagnosis, symptoms, clinical history, current treatment, and existing lab results. Participants will also be asked to submit copies of their most recent blood work and lab results. No intervention or treatment is involved. All data is de-identified.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Female

Aged 18 to 45 years

Diagnosed with Polycystic Ovary Syndrome (PCOS) by a licensed healthcare provider

Willing to voluntarily share existing lab results and clinical history

Disqualifiers

Under 18 years of age

Over 45 years of age

No confirmed PCOS diagnosis from a licensed healthcare provider

Unable or unwilling to provide informed consent

Trial population

Women aged 18 to 45 who have been diagnosed with Polycystic Ovary Syndrome (PCOS) by a licensed healthcare provider. Participants are recruited globally with no geographic restriction. All participants must have a confirmed diagnosis and be willing to voluntarily submit existing lab results and clinical history.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • No intervention - observational data collection only

    Other intervention

    This is an observational study. No intervention or treatment is administered. Participants submit existing lab results and clinical history through an online questionnaire.

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: PCOS Cohort1 intervention

Trial outcomes

Primary outcomes

1

Computational Reconstruction of the Causal Architecture of PCOS

Reconstruction of the hormonal, metabolic, and clinical architecture of Polycystic Ovary Syndrome across the study cohort using computational analysis of participant-submitted lab results and clinical data.

Time frame
Upon completion of data collection, approximately 2 months from study start

Secondary outcomes

1

Identification of Architectural Patterns Across PCOS Cohort

Identification and characterization of distinct architectural patterns across participant cohorts based on hormonal, metabolic, thyroid, lipid, and inflammatory marker profiles.

Time frame
Upon completion of data analysis, approximately 2 months from study start
2

Assessment of Current Treatment Approaches Relative to Causal Architecture

Evaluation of the relationship between participants' current treatment approaches and the underlying causal architecture identified through computational reconstruction.

Time frame
Upon completion of data analysis, approximately 2 months from study start

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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