Clin2
NCT05934487Possibly a fitRecruiting

Monitoring device trial for stable heart failure symptoms

Heart Failure NYHA Class IIHeart Failure NYHA Class IIIHeart Failure

Part of Heart & circulation clinical trials.

This trial tests whether a wearable home monitoring system (myCordella™) can help people with moderate heart failure (NYHA class II or III) by tracking heart pressure and supporting follow-up care. It may help detect changes earlier so clinicians can adjust treatment sooner.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,750 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are at least 18 years old and can give written consent
  • You have heart failure (HF) diagnosed for at least 3 months and are NYHA class II or III
  • Your heart failure medicines have been stable for at least 30 days (or you can’t take them due to documented reasons)
  • You’ve had HF-related hospitalization recently if you’re in the NYHA II or NYHA III group
  • You take a diuretic (“water pill”) for at least 1 month (at a dose equivalent to 40 mg furosemide or more)
  • You can safely use the myCordella™ Patient Reader at home and come back for scheduled visits

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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