Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07043166

Cardiovascular-Kidney-Metabolic Syndrome in Shanghai Zicitizens

Led by Shanghai Changzheng Hospital · Updated on 2025-09-08

4094

Participants Needed

1

Research Sites

547 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main purpose of this study is to conduct follow-up assessments and update the cardiorenal outcomes among the STONE cohort that was established during 2016-2017. The secondary aim is to compare metabolic risk factors, metabolic disturbances, and clinically relevant metabolic outcomes between the follow-up period and the baseline assessment. The exploratory goal is to examine the relationships between changes in risk factors and clinical outcomes in the participants. The study is planned to begin in May 2025 and will finalize the data collection for the entire population by June 2026. During this time, participants will be categorized based on CKM staging. The follow-up phase will continue until 2035.

CONDITIONS

Official Title

Cardiovascular-Kidney-Metabolic Syndrome in Shanghai Zicitizens

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Residents of Shanghai communities enrolled in the STONE cohort
  • Completed baseline questionnaire, physical exam, and clinical tests between 2016 and 2017 with complete data
  • Willing to participate in the follow-up study and provide informed consent
Not Eligible

You will not qualify if you...

  • Moved away from original community and lived elsewhere for more than two years
  • Contact information changed or invalid, making participant uncontactable after three attempts

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai Changzheng Hospital

Shanghai, Shanghai Municipality, China, 200003

Actively Recruiting

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Research Team

T

tuo Tuo Li, Doctor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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