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RecruitingHeart Failure

Mechanisms of Diuretic Resistance in Heart Failure, Aim 1

Eligible age

18+ yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

This study will employ a randomized order, double-blind, repeated measures dose ranging design. This design was chosen in order to generate multiple within-subject serial loop diuretic dose response exposures. The overall study schema will include 75 heart failure (HF) patients.

Sponsor: Yale University

You may qualify if…

  • Clinical diagnosis of HF
  • No plan for titration/change of heart failure medical or device therapies during the study period.
  • Absence of non-elective hospitalizations in the previous 3 months.
  • At optimal volume status by symptoms, exam, and dry weight
  • Age \> 18 years

You may not qualify if…

  • GFR \<20 ml/min/1.73m2 using the Chronic Kidney Disease- Epidemiology (CKD-EPI)equation or use of renal replacement therapies
  • Use of any non-loop type diuretic in the last 14 days with the exclusion of low dose aldosterone antagonist (e.g., spironolactone or eplerenone ≤50 mg). Examples of non-loop diuretics include but may not be limited to acetazolamide (oral or IV, not ophthalmic), metolazone, Hydrochlorothiazide (HCTZ), chlorthalidone, chlorothiazide, indapamide, triamterene, amiloride, finerenone, spironolactone dose \> 50mg day, eplerenone \> 50mg/day,
  • History of flash pulmonary edema requiring hospitalization and treatment with biphasic positive airway pressure or mechanical ventilation or a "brittle" volume sensitive HF phenotype such as an infiltrative or restrictive cardiomyopathy (i.e. amyloid cardiomyopathy, etc).
  • Hemoglobin \< 8 g/dL
  • Pregnant or breastfeeding
  • Inability to give written informed consent or comply with study protocol or follow-up visits
  • Chronic Urinary retention limiting ability to perform timed urine collection procedures

Where it's recruiting

Connecticut

New Haven

Source: ClinicalTrials.gov · NCT05323487 · last updated 2026-05-22