Clinical trial Recruiting at 3 sites Observational Ages 18 and up

A registry for cardiovascular bio-imaging and multi-omics data

Official title: Dongzong Cardiovascular Bio-imaging Registry Study

Run by Jinling Hospital, China · NCT06894095 · Data updated 2026-11-12

This study is trying to collect and analyze different types of health data from adults who have had heart imaging to see how genetics and environment affect heart disease and find ways to prevent and manage it.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment50000 (estimated)
SponsorJinling Hospital, China
Academic / other
Locations3 sites (Nanjing, Jiangsu and 2 other locations)
StatusRecruiting
StartedMay 24, 2023
Main results expectedMarch 31, 2028
Study endsMay 31, 2038
Registry record updatedOctober 16, 2026
Trial IDNCT06894095 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older who have undergone coronary CT angiography.

Probably not a fit

Patients with serious chronic kidney disease, liver dysfunction, or those unable to complete follow-up may not benefit from this study.

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

What this trial studies

The DAILY project is a large-scale, multicenter initiative aimed at creating a comprehensive bio-imaging database that integrates various data types, including living environments, psychosocial assessments, advanced imaging, and multi-omics profiles. This observational study seeks to understand the complex interactions between genetic and environmental factors that influence cardiovascular diseases (CVD). By analyzing these multidimensional datasets, the project aims to identify critical intervention points for the prevention and management of CVD. The study includes participants aged 18 and older who have undergone coronary CT angiography and have provided informed consent.

Why it matters

Potential benefit: If successful, this project could lead to innovative strategies for preventing and managing cardiovascular diseases.

How similar studies have gone: While the integration of multi-omics and bio-imaging is a novel approach, similar studies have shown promise in understanding cardiovascular diseases.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged ≥18 years
* Coronary CT angiography performed
* Informed consent acquired

Exclusion Criteria:

* Unable to complete the follow-up
* Serious chronic kidney disease (eGFR\< 30 ml/min/1.73 m2)
* Serious liver disease or dysfunction (chronic active hepatitis and cirrhosis, or aspartate aminotransferase (AST) or alanine transaminase (ALT) \> 3 times the upper limit of normal)
* Not appropriate to be tested due to birth planning, allergies, acute thyroid storm, etc.
* Suspected or known infectious diseases, such as hepatitis B virus (HBV), human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS), and Treponema pallidum (syphilis), etc.

Where it's running

  • Longjiang Zhang
    Nanjing, Jiangsu, China
    Recruiting
  • Longjiang Zhang
    Suqian, Jiangsu, China
    Recruiting
  • Longjiang Zhang
    Zhenjiang, Jiangsu, China
    Recruiting

Study contacts

  • Principal investigator: Longjiang Zhang, MD — Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University
  • Study coordinator: Longjiang Zhang, MD
  • Email: kevinzhlj@163.com
  • Phone: 13405833167

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.