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Cardiovascular Imaging and Biomarker Analyses (CIBER)

Cardiovascular Imaging and Biomarker Analyses (CIBER)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03074253
Acronym
CIBER
Enrollment
500
Registered
2017-03-08
Start date
2014-12-01
Completion date
2021-07-01
Last updated
2019-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Heart Diseases, Heart Failure

Brief summary

Cardiovascular Imaging and Biomarker Analyses (CIBER) is a single-center, prospective and observational study evaluating the expression of novel biomarkers in patients undergoing cardiacvascular imaging within clinical routine care. It is aimed to evaluate associations with biomarker expressions with ascertained cardiac imaging parameters.

Detailed description

Cardiovascular Imaging and Biomarker Analyses (CIBER) is a single-center, prospective and observational study evaluating the expression of novel biomarkers in patients undergoing cardiacvascular imaging within clinical routine care. It is aimed to evaluate associations with biomarker expressions with ascertained cardiac imaging parameters. Furthermore the prognostic value of biomarkers and imaging parameters on mid-term and long-term prognosis will be evaluated. Novel biomarkers will comprise blood derived biomarkers including neurohormones, proteins, cytokines, microRNAs and metabolomics.

Interventions

DIAGNOSTIC_TESTEchocardiography

Patients are undergoing echocardiography

DIAGNOSTIC_TESTmagnetic resonance imaging

Patients are undergoing magnetic resonance imaging

DIAGNOSTIC_TESTcomputed tomography

Patients are undergoing computed tomography

DIAGNOSTIC_TESTblood withdrawl

Peripheral blood samples are being collected from all patients

Sponsors

Universitätsmedizin Mannheim
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients with low to intermediate risk for coronary artery disease

Exclusion criteria

* under 18 years * mechanical heart valve * pulmonary embolism * deep vein thrombosis * myocardial infarction within the last 3 months * electrical cardioversion within 30 days * status after heart transplant * transient ischemic attack (TIA) or stroke within last 30 days * intracerebral bleeding within the last 2 months * acute infection * existing or planned pregnancy * chronic kidney disease with eGFR \< 40 ml/min

Design outcomes

Primary

MeasureTime frame
Biomarker levels before cardiac imaging24 hours before cardiac imaging

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026