Clinical trial Recruiting at 1 site Observational Ages 18 to 85

Predicting outcomes for people with cardiovascular-kidney-metabolic syndrome

Official title: A Prospective Cohort Study on Prognostic Factors in Patients With Cardiovascular-kidney-metabolic Syndrome

Run by Peking University Third Hospital · NCT07327606 · Data updated 2026-11-12

This project will test whether blood-based molecular markers and heart imaging can help predict outcomes for people with cardiovascular-kidney-metabolic syndrome.

More Cardiovascular-kidney-metabolic Syndrome trials

Quick facts

Study typeObservational
Ages18 Years to 85 Years
SexAll
Enrollment4526 (estimated)
SponsorPeking University Third Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedMay 1, 2025
Main results expectedFebruary 28, 2026
Study endsJune 30, 2027
Registry record updatedJanuary 8, 2026
Trial IDNCT07327606 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults meeting criteria for CKM stages 0–4 with complete clinical data who can undergo adenosine stress echocardiography and regular follow-up are the intended participants.

Probably not a fit

Patients with active infections, autoimmune disease, cancer, life expectancy under two years, known adenosine hypersensitivity, inability to follow up, or who are pregnant or breastfeeding are unlikely to benefit from participation.

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

What this trial studies

This prospective cohort will enroll patients with cardiovascular-kidney-metabolic syndrome and collect clinical data, plasma, and whole blood for transcriptomic, proteomic, and metabolomic analysis. Participants will undergo adenosine stress echocardiography to gather detailed cardiac function data and will be followed long term for clinical outcomes. Modern information technology and bioinformatics will be used to link biomarkers and imaging with prognosis and to build a predictive model that combines molecular and clinical information. The goal is to refine risk stratification and guide personalized treatment and follow-up strategies for CKM patients.

Why it matters

Potential benefit: If successful, the work could allow clinicians to better predict who is at higher risk and tailor treatments and follow-up for people with CKM.

How similar studies have gone: Related biomarker and imaging studies in heart, kidney, and metabolic diseases have shown promise, but integrating multi-omics with stress echocardiography for CKM prognosis is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 1)Patients who meet the criteria for CKM stages 0-4 were included. 2)Clinical data were complete.

Exclusion Criteria:

* 1\) Presence of infectious diseases during the sample retention period. 2) Presence of autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis, systemic sclerosis, vasculitis, etc.

  3\) Presence of tumors. 4) Patients with an estimated life expectancy of less than 2 years. 5) Patients with known hypersensitivity to adenosine. 6) Patients who cannot follow up regularly. 7) Pregnant or breastfeeding women, and those participating in other clinical trials.

Where it's running

  • Peking University Third Hospital
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.