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A Registry Study of Biomarkers in Ischemic Heart Disease ( BIOMS-IHD )

A Registry Study of Biomarkers in Ischemic Heart Disease ( BIOMS-IHD )

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05965882
Enrollment
5000
Registered
2023-07-28
Start date
2016-06-30
Completion date
2024-06-30
Last updated
2024-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases

Keywords

Ischemic heart disease

Brief summary

The registry study aims to discover biomarkers for accurate classification and risk assessment of ischemic heart disease.

Detailed description

The purpose of this study is to discover biomarkers for early identification, diagnosis, molecular classification, and intervention based on the mechanism of ischemic heart disease(IHD). Using mass spectrometry-based metabolomics and multimodal imaging technology, the study aims to further construct a new system for early risk stratification of IHD based on abnormal metabolites.

Interventions

None listed

Sponsors

Beijing Luhe Hospital
CollaboratorOTHER
The First Affiliated Hospital of Shanxi Medical University
CollaboratorOTHER
Beijing Institute of Heart, Lung and Blood Vessel Diseases
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

: * Aged 18 years or older. * Previous ischemic symptoms/signs or electrocardiographic ischemic changes and. * \>70% stenosis of at least one epicardial coronary artery on angiography or a history of myocardial infarction or coronary revascularization.

Exclusion criteria

* Current known inability to follow instructions or comply with follow-up procedures. * Eligible patients without informed consent form

Design outcomes

Primary

MeasureTime frameDescription
Number of hospitalizations for acute heart failure (HF)These data is collected during follow-up visit at 3/6/12/24/36/48 months after dischargeUnplanned emergency visits or hospitalizations leading to HF deterioration were defined as hospitalizations for HF

Secondary

MeasureTime frameDescription
Number of major adverse cardiovascular events (MACE)These data is collected during follow-up visit at 3/6/12/24/36/48 months after dischargeMajor adverse cardiovascular events (MACE) in overall population, defined as composite of all-cause death, Heart Failure hospitalization, recurrent myocardial infarction, stroke or ischemia-driven revascularization.

Countries

China

Contacts

Primary ContactYuan Wang, PhD
wangyuan980510@163.com13910161443
Backup ContactYangkai Fan, PhD
fan@mail.ccmu.edu.cn15010188587

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026