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Withdrawn NCT05633758

Metolazone As Early Add On Therapy For Acute Decompensated Heart Failure

Conditions: Acute Decompensated Heart Failure

Sex: All
Ages: 18 Years – N/A
Phase: PHASE2
Sponsor: Scripps Health

Location: United States

Summary

The primary objective of the study is to determine efficacy of metolazone as synergistic therapy with Lasix in patients with acute decompensated heart failure. This will be a multicenter double blinded randomized placebo- controlled pilot study of the addition of 5 mg of metolazone per day for 2 days compared to placebo in patients admitted with acute decompensated heart failure.

Eligibility Criteria

Inclusion Criteria:Subject is 18 years of age at time of enrollment.Admitted with acute decompensated heart failure based on history, physical exam, and laboratory parameters, must include both:At least 1 symptom of either dyspnea, orthopnea, or edema.At least 1 sign of rales on auscultation, peripheral edema, ascites, or pulmonary vascular congestion on chest radiography.Be willing to comply with protocol-specified instructionsAble to understand and grant informed consent.Exclusion Criteria:Inability to give informed consent.Systolic BP < 90 mmHgCreatinine clearance less than 20ml/min or creatinine greater than 2.5mg/dl.Serum Sodium less than 128meq/L, potassium levels less than 3.5meq/LKnown adverse reaction to metolazoneInability to take oral medicationsSevere Aortic Stenosis (AVA < 0.8cm³)History of Hypertrophic Obstructive Cardiomyopathy.Metastatic CarcinomaSevere Chronic Obstructive Pulmonary Disease (COPD), FEV < 1LSevere dyspnea requiring prolonged CPAP or intubationModerate/Severe Dementia

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05633758). StuddyBuddy aggregates publicly available trial information.