NCT06944405Not yet recruiting
Implementation for Heart Failure Therapies Post-discharge Followed by CardiOSIgnal at HOME
Source: ClinicalTrials.gov · Last updated 25 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
CardioSignal technology (mechanocardiography) could enable home follow-up after admission for acute heart failure, thus improving guidline-directed medical therapies for heart failure dose escalation while reducing the logistical constraints and stress associated with frequent hospital visits. The intended purpose is to detect signs of HF in adults (aged 18 years or older and \< 85 years)
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 65 (estimated)
- First submitted
- 15 Apr 2025
- Start date
- 10 May 2025
- Primary completion date
- 31 Jan 2026
- Lead sponsor
- Precordior Ltd
- Diseases
- Heart failure
- NCT number
- NCT06944405
What you commit to
- Study type: Interventional
- Planned participants: 65
- From 10 May 2025 to the primary completion date, 31 Jan 2026
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous history of allergic asthma at an early age.
Other illness
- Patients with a history of pulmonary embolism.
- Cardiorespiratory disorders which may be aggravated by the slight compression of the thorax. (patient with a pacemaker).
- Known allergies for: bisoprolol, ramipril, Entresto, spironolactone, empagliflozine, dapagliflozine.
Age
- Patients \<18 years and \>85 years.
Other
- Pregnant women. lactating woman.
- The participant's inability to adhere to study procedures or give informed consent.
Who the study is looking for
- Patients admitted at emergency room for acute heart failure.
- Patients discharged from emergency room after an episode of acute heart failure.
- Either LVEF\>40% or ≤40%, either known or assessed during the index hospitalization (however at least 1/3 of patients are required from each category).
- BNP \> 200 pg/ml OR NT-ProBNP \> 800 pg/ml
- Patients with connected smartphone.
Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Fattouma Bourguiba University Hospital, Emergency department Coordinator of this site? Confirm its status | Monastir | Tunisia | Unknown status |
| Sahloul Hospital, Emergency department Coordinator of this site? Confirm its status | Sousse | Tunisia | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.