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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02793180 |
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Date of registration:
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15/05/2016 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Documentation of Heart Failure in a Gulf Registry
DYSPNEA |
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Scientific title:
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Gulf Documentation of Ambulatory Sick Patients With Heart Failure Registry |
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Date of first enrolment:
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November 7, 2016 |
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Target sample size:
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3680 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02793180 |
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Study type:
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Observational [Patient Registry] |
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Study design:
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Phase:
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Countries of recruitment
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Kuwait
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Contacts
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Name:
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Mohammad Zubaid |
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Address:
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Telephone:
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Email:
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Affiliation:
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Gulf Heart Association |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Is over the age of 21.
2. Has been diagnosed with heart failure, regardless of cause.
3. Is presenting to the outpatient clinic of an internist or cardiologist for follow up.
4. Provides a written consent.
Exclusion Criteria:
1. Prior enrolment in this study.
2. Refusal or inability to provide consent.
Age minimum:
21 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Heart Failure
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Primary Outcome(s)
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Quantifying the causes of heart failure in the ambulatory patients in the outpatient setting
[Time Frame: Single time point at baseline upon inclusion (cross-sectional)]
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Secondary Outcome(s)
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Measure investigations that heart failure patients undergo
[Time Frame: Up to 6 months before inclusion]
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Measuring Management Gaps in heart failure patients
[Time Frame: Past 12 months upon inclusion]
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Relationship between cardiovascular risk factors and heart failure
[Time Frame: Single time point at baseline upon inclusion (cross-sectional)]
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Measuring patient functional status in heart failure patients
[Time Frame: Single time point at baseline upon inclusion (cross-sectional)]
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Secondary ID(s)
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CLCZ696BKW01T
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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