Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
500 participants
OBSERVATIONAL
2018-01-01
2022-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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NC
Patients without heart failure.
No interventions assigned to this group
DCM
Dilated cardiomyopathy patients.
No interventions assigned to this group
ICM
Ischemic cardiomyopathy patients.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* enlarged left ventricular end-diastolic dimension
* ICM group: with history of MI or revascularization; ≥ 75% stenosis of LM or proximal LAD; ≥ 75% stenosis of two or more epicardial vessels.
* symptomatic heart failure
Exclusion Criteria
* Pregnancy or lactation period;
* Investigators think not suitable to participate in this trial.
15 Years
80 Years
ALL
No
Sponsors
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Shanghai Zhongshan Hospital
OTHER
Responsible Party
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Locations
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Zhongshan Hospital
Shanghai, , China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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HF201801
Identifier Type: -
Identifier Source: org_study_id
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