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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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9 January 2017 |
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Main ID: |
NCT03009552 |
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Date of registration:
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28/12/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Speckle Tracking Echocardiography Adds Information in Decompensated Heart Failure
STRAIN-DHF |
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Scientific title:
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Speckle Tracking Echocardiography Adds Information in Decompensated Heart Failure |
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Date of first enrolment:
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June 2016 |
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Target sample size:
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176 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03009552 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Phase:
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N/A
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Countries of recruitment
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Brazil
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Contacts
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Name:
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Marco Stephan L Alves, MD |
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Address:
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Telephone:
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+55 11 26615646 |
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Email:
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mslalves@hotmail.com |
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Affiliation:
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Name:
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Marco Stephan L Alves, MD |
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Address:
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Telephone:
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+55 11 981431512 |
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Email:
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mslalves@hotmail.com |
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Affiliation:
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Name:
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Marco Stephan L Alves, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Sao Paulo |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Admission in the emergency for decompensated heart failure.
Exclusion Criteria:
- Systolic blood pressure < 85, need surgical treatment, high ventricular frequency
atrial fibrillation or flutter, severe pulmonary disease, pulmonary embolism, septic
shock, advanced malignant neoplasia, pregnancy, heart transplant.
Age minimum:
18 Years
Age maximum:
75 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Decompensated Heart Failure
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Intervention(s)
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Procedure: speckle tracking echocardiography
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Primary Outcome(s)
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Composite endpoint of mortality, heart transplant, left ventricular assist device and readmission for decompensated heart failure.
[Time Frame: Six months after admission]
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Secondary Outcome(s)
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Development of cardio-renal syndrome (loss of more than 30% of calculated creatinine clearance or need for dialysis)
[Time Frame: 1 month after admission]
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Cardiac mortality
[Time Frame: 6 months]
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Secondary ID(s)
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2015/10005-5
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CAAE:59669416.0.0000.0068
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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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