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Taking people in ChinaNo phase

Following adults with combined heart, kidney and metabolic disease over time

Follows adults with heart, kidney or metabolic disease for up to 5 years.

Plain-language title generated from the registry record
Registry title: Study on Construction of Whole Lifecycle Cohort, Big Data Management and Clinical Prognosis of Cardio-Renal-Metabolic (CKM) Syndrome

Key facts

Where
Fuzhou, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07547098, who can take part

Where in China

  • The First Affiliated Hospital of Fujian Medical UniversityFuzhou, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
First Affiliated Hospital of Fujian Medical University
Trial code
NCT07547098
Record updated
23 April 2026
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: 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; Ability to complete baseline assessment and follow-up; Full civil capacity and ability to understand study information.

Exclusion: Severe psychiatric disease or cognitive impairment precluding participation; End-stage disease with expected survival less than 1 year; Refusal to provide written informed consent; Long-term absence more than 6 months preventing reliable follow-up; Participation in another clinical study that may interfere with endpoint adjudication; Missing key fields preventing linkage of examinations, imaging, and outcomes.

ClinicalTrials.gov NCT07547098