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Clinical Trials/NCT03905252
NCT03905252
Completed
Not Applicable

Biomarkers for Human Heart Failure

Mayo Clinic1 site in 1 country535 target enrollmentAugust 2009
ConditionsCHF

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
CHF
Sponsor
Mayo Clinic
Enrollment
535
Locations
1
Primary Endpoint
uAGT levels in high-risk chronic HF patients
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to establish the various ranges of proteins that can be assayed in the plasma and urine from hospitalized patients with all classes of heart failure and/or STEMI (ST-segment elevation myocardial infarction)/NSTEMI (Non-ST-segment elevation myocardial infarction), as well as history reviews.

Detailed Description

Schematic Design of the Study: Single blood draw, one random urine and 24-hr urine collection from hospitalized patients with chronic/acute heart failure and/or STEMI-NSTEMI. If there should be a subsequent hospitalization,another collection of a 45 ml blood sample, random urine and one 24-hour urine collection may be completed if indicated at initial hospitalization. Aims: The purpose of this study is to attempt to establish the various ranges of proteins that can be assayed from the plasma and urine of patients with all classes of heart failure and MI (myocardial infarction). Follow-up hospitalizations may result in another 45 ml blood draw, random urine and 24-hr. urine collection to evaluate the outcome of the heart failure treatment used with the previous hospitalization, if indicated in consent. A history review will be necessary as well.

Registry
clinicaltrials.gov
Start Date
August 2009
End Date
February 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

John C Burnett

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of Acute decompensated heart failure

Exclusion Criteria

  • Hemoglobin less than 10, active cancer, or amyloidosis Patient with dialysis

Outcomes

Primary Outcomes

uAGT levels in high-risk chronic HF patients

Time Frame: 10 years

This study will provide new knowledge of the pathology and outcomes predicted by the use of uAGT in symptomatic chronic HF patients at high risk for future hospitalization and death.

Natriuretic peptide levels in ADHF patients

Time Frame: 20 years

new knowledge of pathology and outcomes in ADHF patients

Study Sites (1)

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