Evaluation of the Effectiveness of the Cardiostory Device in Distinguishing Heart Failure From Other Causes in Patients Presenting With Dyspnea.

Recruiting now

Conditions studied: Heart Failure, Dyspnea

In brief

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.

Key facts

Study ID

NCT07685106

Run by

CardioStory INC

People needed

850

Starts

2025-09-01

Expected to finish

2026-12-01

Last updated by the study team

2026-07-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years
• Recent onset dyspnea (less than 7 days)
• Informed consent obtained

You may not qualify if…

• 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

• Fattouma bourguiba university hospital — Monastir, Monastir Governorate, Tunisia (enrolling)
• Sahloul university hospital — Sousse, Tunisia (enrolling)

Full record on ClinicalTrials.gov

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