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Continuous Versus Bolus Intermittent Loop Diuretic Infusion in Acutely Decompensated Heart Failure: Evaluation of Renal Function, Congestion Signs, BNP and Outcome

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

DiurHF is a prospective, multicenter, observational, study that compares continuous with intermittent infusion of furosemide in patients admitted with a diagnosis of ADHF. Previous pilot study design was planned to anticipate a larger multicenter trial able to definitively evaluate the optimal loop diuretic use strategy in patients with ADHF.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients over 18 years;

• Patients with diagnosis of ADHF(dyspnea, orthopnea, peripheral edema or major fatigue and at least two clinical signs including rales, hepatomegaly, pulmonary congestion on chest radiography, jugular vein dilatation, or a third heart sound);

• Blood BNP \> 100 pg/mL;

⁃ ADHF: Acute Decompensated Heart Failure; BNP: B-type Natriuretic Peptide; IV: IntraVenous; LVEF: Left Ventricular Ejection Fraction.

Locations
Other Locations
Italy
Ospedale Madonna della Navicella
RECRUITING
Chioggia
Azienda Ospedaliera di Padova
RECRUITING
Padova
University of Rome La Sapienza
RECRUITING
Roma
Department of Internal Medicine, Cardiovascular Diseases Unit
RECRUITING
Siena
Contact Information
Primary
Alberto Palazzuoli, MD
palazzuoli2@unisi.it
+390577585363
Backup
Gaetano Ruocco, MD
gmruocco@virgilio.it
+393386577898
Time Frame
Start Date: 2015-12
Estimated Completion Date: 2028-01
Participants
Target number of participants: 370
Treatments
Continuous Furosemide Infusion
continuous intravenous furosemide infusion
Intermittent Furosemide Infusion
bolus intermittent intravenous furosemide infusion
Related Therapeutic Areas
Sponsors
Collaborators: University of Milan, Ospedale Regina Montis Regalis, A.O.U. Città della Salute e della Scienza, University of Roma La Sapienza, University of Naples
Leads: University of Siena

This content was sourced from clinicaltrials.gov