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

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.

NCT Number	NCT07685106
Lead Sponsor	CardioStory INC Collaborators: Eshmoun Clinical Research Center, Sahloul Hospital of Sousse, University Hospital Monastir, Tunis
Conditions	Heart Failure, Dyspnea
Enrollment	850 participants
Start Date	2025-09-01
Primary Completion	2026-12 (estimated)
Study Completion	2026-12 (estimated)
Updated on ClinicalTrials.gov	2026-07-06