Clinical Trials Directory

Trials / Recruiting

RecruitingNCT02901184

Spironolactone Initiation Registry Randomized Interventional Trial in Heart Failure With Preserved Ejection Fraction

Spironolactone Initiation Registry Randomized Interventional Trial in Heart Failure With Preserved Ejection Fraction, SPIRRIT-HFPEF

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
2,000 (estimated)
Sponsor
Uppsala University · Academic / Other
Sex
All
Age
50 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Heart failure with preserved ejection fraction (HFPEF) is common and deadly but without therapy. Inconclusive studies such as TOPCAT (Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist) suggest spironolactone may be effective in HFPEF, but it is generic and will not be studied by industry. SPIRRIT is a unique Registry-Randomized Clinical Trial (RRCT) that will test the hypothesis that spironolactone plus standard of care compared to standard of care alone reduces the composite of CV mortality and HF hospitalization as follows: Population: HFPEF patients in the Swedish Heart Failure Registry and HFPEF patients in US. HFPEF defined as symptoms/signs of HF, elevated NTproBNP (B-type Natriuretic Peptide; N-terminal pro b-type Natriuretic Peptide) and EF\>=40%. Intervention and control: Randomized 1:1 to intervention: spironolactone + usual care vs. control: usual care alone. Outcome: Primary outcome cardiovascular death or time to HF hospitalization. Secondary outcomes include hospitalization for various causes, adverse events and treatment adherence. In Sweden outcomes are obtained automatically by linking with the Population, Patient and Drug Dispensed Registries. In the US, outcomes will be reported by sites and supplemented by data from a call center. The trial is event-driven with enrollment 7 years and study duration 9 years. For the primary outcome (CV Death or first HF hospitalization) with an event target of 721 events the sample size requires 1985 patients conservatively rounded to approximately 2000 patients.

Conditions

Interventions

TypeNameDescription
DRUGSpironolactoneTreatment with Spironolactone tablets on top of standard care
OTHERStandard careStandard care does not involve Spironolactone

Timeline

Start date
2017-11-23
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2016-09-15
Last updated
2024-10-22

Locations

78 sites across 2 countries: United States, Sweden

Regulatory

Source: ClinicalTrials.gov record NCT02901184. Inclusion in this directory is not an endorsement.