Strain for Risk Assessment and Therapeutic Strategies in Patients With Acute Heart Failure (STRATS-AHF) Registry (STRATS-AHF)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03513653 |
Recruitment Status :
Active, not recruiting
First Posted : May 1, 2018
Last Update Posted : October 22, 2020
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Condition or disease | Intervention/treatment |
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Heart Failure Acute Heart Failure Echocardiography | Diagnostic Test: Echocardiography with speckle-tracking imaging |
Study Type : | Observational |
Actual Enrollment : | 4312 participants |
Observational Model: | Cohort |
Time Perspective: | Retrospective |
Official Title: | Strain for Risk Assessment and Therapeutic Strategies in Patients With Acute Heart Failure (STRATS-AHF) Registry |
Actual Study Start Date : | January 1, 2009 |
Actual Primary Completion Date : | September 5, 2017 |
Estimated Study Completion Date : | December 31, 2022 |

Group/Cohort | Intervention/treatment |
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Acute heart failure
Patients hospitalized for acute heart failure and underwent echocardiography with speckle-tracking imaging
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Diagnostic Test: Echocardiography with speckle-tracking imaging
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- All-cause mortality [ Time Frame: up to 5 years ]Death from any cause
- Hospitalization for heart failure [ Time Frame: up to 5 years ]Any hospitalization for acute heart failure after the index hospitalization
- Composite of all-cause mortality and hospitalization for heart failure [ Time Frame: up to 5 years ]Death from any cause or any hospitalization for acute heart failure after the index hospitalization
- Ischemic stroke [ Time Frame: up to 5 years ]Ischemic stroke (an episode of neurological dysfunction caused by embolism) after the index hospitalization

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Inclusion Criteria:
- Patients with signs or symptoms of HF and either lung congestion, or objective findings of LV systolic dysfunction or structural heart disease
Exclusion Criteria:
- Patients who presented with acute coronary syndrome

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03513653
Korea, Republic of | |
Seoul National University Bundang Hospital | |
Seongnam-si, Gyeonggi-do, Korea, Republic of, 13620 | |
Chungnam National University Hospital | |
Daejeon, Korea, Republic of, 35015 | |
Seoul National University Hospital | |
Seoul, Korea, Republic of, 03080 |
Principal Investigator: | Goo-Yeong Cho, MD, PhD | Seoul National University Bundang Hospital |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Goo-Yeong Cho, Professor, Seoul National University Bundang Hospital |
ClinicalTrials.gov Identifier: | NCT03513653 |
Other Study ID Numbers: |
B-1702/384-111 |
First Posted: | May 1, 2018 Key Record Dates |
Last Update Posted: | October 22, 2020 |
Last Verified: | October 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
acute heart failure global longitudinal strain ejection fraction echocardiography mortality |
Heart Failure Heart Diseases Cardiovascular Diseases |