Sequential Cystatin C Levels and Renal Impairment in Acute Heart Failure
NCT00561483
Acute Heart Failure, Female Urogenital Diseases
Cleveland, Ohio, United States
View Trial DetailsNCT Number: NCT00514384
Evaluation of serial measurement of novel biomarker for diagnosis, prognosis or therapy monitoring in patients presenting with acute decompensated heart failure.
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Notify Me18 year and older
All sexes
Observational
Cantonal Hospital Aarau, Aarau, Canton of Aargau, Switzerland
Background: Heart failure (HF) is a chronic and progressive illness resulting from a variety of cardiac causes, including ischemic and valvular heart disease, dilatative cardiomyopathy or hypertension. HF may also develop suddenly, particularly as a complication of acute myocardial infarction or as an acute exacerbation in patients with previously compensated chronic HF. Diagnosis and in-hospital management of HF is often demanding and outcome especially regarding rehospitalizations is impaired. Novel biomarker may be very helpful in assessment of diagnosis, prognosis, and severity of HF as well as for treatment monitoring.
Design: Prospective, multicenter observational study Setting: University Hospital Basel, Kantonsspital Aarau, Kantonsspital Luzern, Kantonsspital Wolhusen Patients: Patients with acute HF not requiring ICU admission
Measurement of serial biomarker (BNP, NT-proBNP, MR-proADM, ST2, hs-cTnI and Copeptin) will be performed at presentation, at 6 hours (h), 12h, 18h, 24h, at 48h, at day 6 and at hospital discharge. Follow- up will be performed at 6 Month, 1 year and 2 years.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Entry, 6h, 12h, 18h, 24h, 48h, 6 days, discharge
University Hospital, Basel, Switzerland
Other
Prognostic Value of Serial Biomarker Measurements in Patients With ADHF
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