NYHA Class II Heart Failure

2

Review clinical trials related to NYHA Class II Heart Failure. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

NORM-HF Pivotal Study

This is an international, multi-center, prospective, randomized, open-label blinded endpoint study designed to demonstrate that use of the FIRE1 NORM™ System in the management of New York Heart Association Class II/III HF patients is superior for reducing the combined endpoint of worsening HF events and cardiovascular mortality compared to standard of care treatment. Patients will be randomized in a 1:1 ratio to receive either NORM™ System and guided heart failure management (intervention group) or usual standard of care with guided heart failure management (control group).

Participants needed: 800
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Foundry Innovation & Research 1, Limited (FIRE1)Updated: Jun 24, 2026Locations: 3
Eligibility criteria

Adults 18 years of age or older. [+9]

Persistent NYHA functional class IV HF (ACC/AHA/ESC). [+21]

Status: Recruiting

Dietary Tracking in Heart Failure

Emerging evidence links ultra processed foods (UPFs) to adverse cardiovascular outcomes. UPFs are often high in sodium, unhealthy fats and added sugars, while being low in essential nutrients and fiber. UPFs contribute to systemic inflammation, fluid retention, and metabolic dysfunction-key drivers of HF and kidney disease progression. Traditional dietary counseling often lacks specificity around food processing levels. Furthermore, the majority of nutrition studies relied on extensive self-reported dietary recall food frequency questionnaires (FFQ) that are subjective, often labor intensive, and difficult to implement practically in the clinical setting. As such, researchers have developed metabolite scores from blood and urine samples to help quantify UPF consumption, which has the promise to better guide dietary counseling and track process. Therefore, the aim of this study is to evaluate the feasibility and physiological impact of a structured UPF-reduction dietary intervention in patients with HF, leveraging both digital dietary tools (Cronometer) and biomarker assessments.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: The Cleveland ClinicUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Adults (≥18 years) with NYHA Class II-III HF [+1]

History of heart transplant or LVAD implant [+2]