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NT-proBNP and New Biomarkers in Patients With Dyspnea and/or Peripheral Edema

Mannheim NT-proBNP Study (MANPRO) Evaluating NT-proBNP and New Biomarkers in Patients Suffering From Dyspnea and/or Peripheral Edema for the Differential Diagnosis of Congestive Heart Failure

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00143793
Acronym
MANPRO
Enrollment
400
Registered
2005-09-02
Start date
2005-06-30
Completion date
2019-12-31
Last updated
2020-08-27

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

Conditions

Dyspnea, Peripheral Edema

Keywords

natruretic peptides, NT-proBNP, new biomarkers, congestive heart failure, atrial fibrillation, acute myocardial infarction, lung embolism

Brief summary

The objectives of this study are to: * Evaluate the sensitivity and specificity of NT-proBNP (N-terminal prohormone brain natriuretic peptide) and new biomarker measurements for the diagnosis of heart failure in patients with acute dyspnea and/or edema. * Determine the exact biomarker cut-off point(s) for the differentiation of healthy persons, patients with heart failure and patients with dyspnea of other origin. * Evaluate treatment costs in patients with dyspnea under special consideration of NT-proBNP measurement.

Detailed description

Primary endpoint: * Sensitivity and specificity of biomarker measurements for discrimination of heart failure from dyspnea of other origin. Secondary endpoints: * Determination of Cut-off(s) * Discrimination of cardiac and non-cardiac diseases causing to dyspnea or peripheral edema * Determination of treatment costs of the initial hospital stay * Evaluation of resource savings when implementing NT-proBNP for determination of diagnosis. * Time to diagnosis. * Hospitalization rate /Intensive care treatment rate between day 1 and 28 * Duration of initial hospital stay * 30-day re-hospitalization rate * 30 day mortality rate and adverse event rate * 1 and 5 year mortality rates * 1 and 5 year rehospitalization rates

Interventions

None listed

Sponsors

Universitätsmedizin Mannheim
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-90 years * Dyspnea or/and peripheral edema * Informed consent

Exclusion criteria

* Renal insufficiency with creatinine \> 2.8mg/dl * Anemia (hemoglobin \< 8.0mg/dl) * Pregnancy

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026