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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02634762
Other study ID # 1
Secondary ID
Status Completed
Phase
First received December 16, 2015
Last updated March 28, 2018
Start date January 2011
Est. completion date December 2017

Study information

Verified date March 2018
Source Institute for Clinical Evaluative Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This prospective validation study evaluates the ability of a risk algorithm, which can simultaneously predict the risk of death at 7 days and 30 days for patients with acute heart failure presenting to the emergency department. The risk algorithms for prediction of 7-day (Emergency Heart failure Mortality Risk Grade [EHMRG]) and 30-day mortality (EHMRG30-ST) have been previously derived.


Recruitment information / eligibility

Status Completed
Enrollment 1983
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with acute heart failure diagnosed in the emergency department

Exclusion Criteria:

- Palliative or do-not-resuscitate (DNR) directive

- Dialysis dependent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Canada University Health Network Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
Institute for Clinical Evaluative Sciences

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality Death within 7 days after emergency department presentation for heart failure 7 days
Primary Mortality Death within 30 days after emergency department presentation for heart failure 30 days
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