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Taking people in CzechiaNo phase

Screening for long-term lung blood clot complications after a pulmonary embolism

Tests a screening program for chronic lung blood clot disease in adults after pulmonary embolism.

Plain-language title generated from the registry record
Registry title: Early Detection of CTEPH in Patients After APE

Key facts

Where
Brno, Havlíčkův Brod, Hradec Králové, Jihlava, Náchod, Olomouc, Ostrava, Pardubice, Rychnov nad Kněžnou, and Tábor, CzechiaSee the 10 sites

Where in Czechia

  • Brno University HospitalBrno, CzechiaTaking people
  • Havlíčkův Brod HospitalHavlíčkův Brod, CzechiaTaking people
  • University Hospital Hradec KraloveHradec Králové, CzechiaTaking people
  • Jihlava HospitalJihlava, CzechiaTaking people
  • Náchod HospitalNáchod, CzechiaTaking people
  • University Hospital OlomoucOlomouc, CzechiaTaking people
  • University Hospital OstravaOstrava, CzechiaTaking people
  • Pardubice HospitalPardubice, CzechiaTaking people
  • Rychnov nad Kněžnou HospitalRychnov nad Kněžnou, CzechiaTaking people
  • Tábor HospitalTábor, CzechiaTaking people

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  4. What happens if I want to stop?
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Trial details

Who runs it
Institute of Health Information and Statistics of the Czech Republic
Trial code
NCT06865326
Record updated
4 November 2026
Original description
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.Read full original descriptionShow less

Early Detection of Chronic Thromboembolic Pulmonary Hypertension in Patients After Acute Pulmonary Embolism

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.

Inclusion: Age over 18 years; Signed consent to participate in the project and GDPR; Patients with an episode of acute pulmonary embolism in the last 3-12 months, with ongoing anticoagulation therapy:; 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; Asymptomatic patients after a pulmonary embolism episode and at least one of the following risk factors:; ECHO evidence of severe PH at diagnosis of PE (PASP >60 mmHg); Antiphospholipid syndrome with triple positivity (presence of lupus anticoagulans + anti-beta-2-glycoprotein I (B2GPI) antibodies + anticardiolipin); Infected permanent venous inlets and cardiac pacing/defibrillation intravascular systems; Presence of ventriculoatrial shunt for treatment of hydrocephalus; Nonspecific intestinal inflammation (ulcerative colitis, Crohn's disease); History of splenectomy; Myeloproliferative disorders; Chronic osteomyelitis.

Exclusion: Not agreeing to participate in the project; Contraindications to treatment.

ClinicalTrials.gov NCT06865326