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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RECRUITING
30000 participants
OBSERVATIONAL
2024-06-01
2028-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Hypertension Hypertension is defined as office systolic blood pressure is ≥ 140mmHg and/or the diastolic blood pressure is ≥ 90mmHg without the use of antihypertensive drugs.
3. Heart failure There is a clear history of organic heart disease, clinical symptoms and signs of heart failure, and objective evidence of heart failure.
4. Cardiomyopathy Including defined dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, etc.
5. Able to sign informed consent form.
Exclusion Criteria
2. Patients with various malignant tumors.
3. Liver dysfunction (defined as ALT or total bilirubin greater than three times the upper normal limit).
4. Renal insufficiency (defined as blood creatinine exceeding 1.5 times the upper normal limit).
5. Those who have participated in other clinical studies within the past three months.
6. Individuals without legal capacity or with limited legal capacity.
7. Any situation where the researcher deems it unsuitable to participate in the clinical study.
18 Years
80 Years
ALL
No
Sponsors
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Xinjiang Medical University
OTHER
Responsible Party
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Xiang Xie
Director
Principal Investigators
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Xiang Xie, Prof
Role: PRINCIPAL_INVESTIGATOR
Xinjiang Medical University
Locations
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The First Affiliated Hospital of Xinjiang Medicial University
Ürümqi, Xinjiang, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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20240606
Identifier Type: -
Identifier Source: org_study_id
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