Evaluation of the Effectiveness of the Cardiostory Device in Distinguishing Heart Failure From Other Causes in Patients Presenting With Dyspnea.
Recruiting · NCT07685106 · Observational (researchers observe without assigning treatment) · Lead sponsor: CardioStory INC
View the official record on ClinicalTrials.gov →Interventions studied
Non invasive cardiac assessment with the CardioStory device
What this trial is about
This is a prospective, observational study conducted in the emergency department. Adult patients presenting with dyspnea will be enrolled, and study data will be collected from routine clinical assessments, including medical history, physical examination, laboratory tests, and echocardiography results, as well as non-invasive cardiovascular measurements obtained using the CardioStory device.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Age ≥ 18 years
- Recent onset dyspnea (less than 7 days)
- Informed consent obtained
Exclusion criteria
- Age inferior to 18 years,
- Severe comorbidity, hemodynamic compromise or immediate need for mechanical ventilation were exclusion criteria.
- Dyspnea clearly of traumatic or allergic origin
Where it is running
2 locations listed.
- Sahloul university hospital - Sousse, Tunisia
- Fattouma bourguiba university hospital - Monastir, Monastir Governorate, Tunisia