RecruitingNot ApplicableNCT04149743
HEMOTAG® Assessment for Short-term Outcomes of Heart Failure
HEMOTAG® Assessment for Short-term Outcomes of Heart Failure [HATS-OFF]
Sponsor
Aventusoft, LLC.
Enrollment
420 participants
Start Date
Jan 31, 2022
Study Type
INTERVENTIONAL
Conditions
Summary
Evaluation of the HEMOTAG® system in a less controlled environment and concurrently develop the system for use by patients with heart failure.
Eligibility
Min Age: 22 Years
Plain Language Summary
Simplified for easier understanding
This study is evaluating a wearable device called HEMOTAG to monitor patients with heart failure after they leave the hospital. The device tracks fluid levels and other markers to help predict whether a patient might need to return to the hospital. The goal is to see if remote monitoring can help doctors intervene earlier and prevent readmissions.
**You may be eligible if...**
- You are 22 years or older
- You have been admitted to the hospital for acute decompensated heart failure (your heart is not pumping well and you have fluid buildup)
- You are receiving IV diuretics or blood pressure medications
- Your BNP or NT-proBNP levels are elevated (indicating heart strain)
- You have cellular data coverage at home
- If you have a history of reduced heart function, you must have been on standard heart failure medications for at least 90 days
**You may NOT be eligible if...**
- You are unable to give informed consent
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
DIAGNOSTIC_TESTStandard of Care with Hemotag
Comparison of outcomes
Locations(2)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT04149743
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