Study on Construction of Whole Lifecycle Cohort, Big Data Management and Clinical Prognosis of Cardio-Renal-Metabolic (CKM) Syndrome

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorFirst Affiliated Hospital of Fujian Medical University

About this trial

This is a single-center observational registry study aiming to establish a structured clinical and multimodal imaging database for cardiovascular-kidney-metabolic (CKM) populations and to support lifecycle follow-up and outcome management. Adult patients aged 18-80 years with cardiovascular, kidney, and/or metabolic diseases or key data for CKM phenotyping will be enrolled at the First Affiliated Hospital of Fujian Medical University. The study integrates retrospective data entry and prospective follow-up, including clinical records, laboratory tests, medications, electrocardiography, echocardiography, vascular function assessment, carotid and abdominal ultrasound, bone density, coronary CTA and post-processing data. The primary outcome is the first occurrence of a cardiorenal composite endpoint. Participants will be followed for up to 5 years through active annual follow-up and passive monthly data updates to support risk stratification, real-world evidence generation, and CKM management pathway optimization.

Eligibility criteria

Qualifiers

Age 18 years or older.

Inpatient record available at the First Affiliated Hospital of Fujian Medical University with retrievable identifiers for data linkage.

Cardiovascular disease, kidney disease, metabolic disease, or key examination/laboratory information supporting CKM phenotyping.

Willingness to participate and provision of written informed consent.

Disqualifiers

Refusal to provide written informed consent.

Severe psychiatric disease or cognitive impairment precluding participation.

End-stage disease with expected survival less than 1 year.

Long-term absence more than 6 months preventing reliable follow-up.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

8,000 Participants
are grouped into 1 trial group