Heart Monitoring Device After Acute Myocardium Infarction
NCT ID: NCT03494751
Last Updated: 2019-04-08
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
NA
358 participants
INTERVENTIONAL
2019-05-01
2020-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Heart Monitor
We used the device (heart monitor) in the patients with myocardial infarction.
Heart monitor
Use of heart monitor device in the patients after acute myocardium infarct.
No Heart Monitor
No heart monitor device in the patients with myocardial infarction (control).
No heart monitor
Standard monitoring by nurses.
Interventions
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Heart monitor
Use of heart monitor device in the patients after acute myocardium infarct.
No heart monitor
Standard monitoring by nurses.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* patients post-acute myocardial infarctium
Exclusion Criteria
* patients with congenital heart disease
18 Years
ALL
No
Sponsors
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Instituto de Cardiologia do Rio Grande do Sul
OTHER
Responsible Party
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Principal Investigators
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silvia goldmeier
Role: STUDY_CHAIR
Instituto de Cardiologia do Rio Grande do Sul
Central Contacts
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Other Identifiers
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5391/17
Identifier Type: -
Identifier Source: org_study_id
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