Early Detection of CTEPH in Patients After APE

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInstitute of Health Information and Statistics of the Czech Republic

About this trial

The project is a national, prospective, multicenter, observational pilot project of screening CTEPH in pacients after APE in the Czech Republic. The main goal of the project is to methodically prepare, implement and evaluate a pilot project that will verify the suitability of the proposed procedure of early detection of Chronic tromboembolic pulmonary hypertesion in such a way as to ensure the maximum positive impact on the health of the population and high cost-effectiveness of the whole process.

Eligibility criteria

Qualifiers

Age over 18 years

Signed consent to participate in the project and GDPR

Patients with new-onset and ongoing or progressive dyspnea (min. NYHA II) after a pulmonary embolism episode or worsening of dyspnea after a pulmonary embolism episode compared to the status before the episode (at least 1 HYHA grade) or

ECHO evidence of severe PH at diagnosis of PE (PASP >60 mmHg)

Disqualifiers

Not agreeing to participate in the project

Contraindications to treatment

Trial design

Treatments tested in this trial

  • Standardized CTEPH Screening Protocol

Treatment groups

500 Participants
are divided into 1 treatment group

Sponsors and collaborators