Clinical trial Recruiting at 1 site Observational Ages 20 and up

Combining genetics, blood, urine, and stool data to predict complications of metabolic syndrome

Official title: Validating Integrative Multi-omics Approaches in Metabolic Syndrome-related Diseases: A Step Towards Precision Medicine

Run by Chang Gung Memorial Hospital · NCT07248371 · Data updated 2026-11-12

The team will try combining genetic, blood, urine, and stool data to see if patterns predict complications in adults with or without metabolic syndrome.

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Quick facts

Study typeObservational
Ages20 Years and up
SexAll
Enrollment6266 (estimated)
SponsorChang Gung Memorial Hospital
Academic / other
Locations1 site (Taoyuan)
StatusRecruiting
StartedJune 9, 2025
Main results expectedSeptember 30, 2028
Study endsSeptember 30, 2035
Registry record updatedNovember 25, 2025
Trial IDNCT07248371 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 20 years or older who can give informed consent, including people who meet diagnostic criteria for metabolic syndrome and age- and sex-matched individuals without metabolic syndrome, are eligible.

Probably not a fit

Pregnant or breastfeeding people, patients on dialysis for end-stage renal disease, those receiving active cancer treatment, organ transplant recipients, or individuals with dementia are excluded and would not benefit from participation in this observational protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This longitudinal, multi-center observational project will enroll adults with metabolic syndrome and age- and sex-matched controls from Chang Gung Memorial Hospitals. Researchers will collect annual blood samples plus urine and stool to generate genomics, transcriptomics, metabolomics, and microbiome profiles and link these to clinical records from the hospital research database. Advanced bioinformatics, dimensionality reduction, clustering, and machine-learning feature selection will be used to integrate the datasets and build models of disease progression and complications. The goal is to identify multi-layer molecular networks and signatures that differentiate patients who develop complications from those who do not.

Why it matters

Potential benefit: If successful, this work could enable earlier, more personalized prevention and treatment by identifying molecular signatures that predict who will develop metabolic complications.

How similar studies have gone: Prior multi-omics research has produced promising biomarker signals for metabolic conditions but few approaches have yet produced broadly validated clinical prediction tools, so this is a promising but still-emerging area.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Individuals (male or female) aged 20 years or older
* Willing and able to provide written informed consent to participate in the study

Exclusion Criteria:

* Pregnant or breastfeeding women
* Patients with end-stage renal disease receiving hemodialysis or peritoneal dialysis
* Individuals currently undergoing active cancer treatment
* Recipients of any organ transplantation
* Patients diagnosed with dementia

Where it's running

  • Chang Gung Memorial Hospitals, Linkou
    Taoyuan, Taiwan
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.