A Registry Study of Biomarkers in Ischemic Heart Disease ( BIOMS-IHD )
1 other identifier
observational
5,000
1 country
1
Brief Summary
The registry study aims to discover biomarkers for accurate classification and risk assessment of ischemic heart disease.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2016
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2016
CompletedFirst Submitted
Initial submission to the registry
July 20, 2023
CompletedFirst Posted
Study publicly available on registry
July 28, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2024
CompletedJanuary 29, 2024
January 1, 2024
8 years
July 20, 2023
January 25, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of hospitalizations for acute heart failure (HF)
Unplanned emergency visits or hospitalizations leading to HF deterioration were defined as hospitalizations for HF
These data is collected during follow-up visit at 3/6/12/24/36/48 months after discharge
Secondary Outcomes (1)
Number of major adverse cardiovascular events (MACE)
These data is collected during follow-up visit at 3/6/12/24/36/48 months after discharge
Eligibility Criteria
Partients with ischemic heart disease accorrding to Inclusion and exclusion criteria.
You may qualify if:
- 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.
You may not qualify if:
- Current known inability to follow instructions or comply with follow-up procedures.
- Eligible patients without informed consent form
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Beijing Anzhen Hospital
Beijing, Beijing Municipality, 100029, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Jie Du, phD
The Key Laboratory of Remodeling-Related Cardiovascular Disease, Ministry of Education, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart,Lung and Blood Vessel Diseases
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 20, 2023
First Posted
July 28, 2023
Study Start
June 1, 2016
Primary Completion
June 1, 2024
Study Completion
June 1, 2024
Last Updated
January 29, 2024
Record last verified: 2024-01