Blood Collection From Heart Failure Patients to Evaluate for Galectin-3 Measurement Differences Using Various Collection Tubes

NCT ID: NCT01980862

Last Updated: 2014-08-05

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

48 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-08-31

Study Completion Date

2013-11-30

Brief Summary

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Single-site blood collection investigation.

Detailed Description

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45 Heart Failure patients will be recruited. Patients will provide a one-time blood sample specimen collection. Theses samples will be de-identified and provided for measurement of Galectin-3 on commercial platforms.

Conditions

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To Measure Galectin-3 in Heart Failure Patients on Commercial Platforms

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Heart Failure patients

No interventions for this study. Blood draw provided by patients.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Heart Failure patients New York Heart Association class able to provide (4) collection tube types Subjects \> 18 years old All subjects must provide informed consent and associated documentation

Exclusion Criteria

* Subjects that cannot tolerate blood withdrawal of 4 specimens collection tube tubes (approximately 40 mLs)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fujirebio Diagnostics, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Robert Christenson, MD

Role: PRINCIPAL_INVESTIGATOR

Universtiy of Maryland School of Medicine

Locations

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University of Maryland School of Medicine

Baltimore, Maryland, United States

Site Status

Countries

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United States

Other Identifiers

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FDI-83

Identifier Type: -

Identifier Source: org_study_id

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