Early Detection of CTEPH in Patients After APE
Launched by INSTITUTE OF HEALTH INFORMATION AND STATISTICS OF THE CZECH REPUBLIC · Mar 5, 2025
Trial Information
Current as of July 27, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a condition called Chronic Thromboembolic Pulmonary Hypertension (CTEPH), which can develop in some patients who have had an episode of acute pulmonary embolism (a blockage in the lung arteries). The main goal of the study is to find out the best ways to detect CTEPH early in patients after they have experienced a pulmonary embolism. This is important because early detection can help improve patients' health and make the healthcare process more effective and affordable.
To participate, you must be over 18 years old and have had a pulmonary embolism in the last 3 to 12 months while receiving blood-thinning medication. You might be eligible if you are experiencing ongoing shortness of breath or if you have certain risk factors, such as a serious heart condition or specific autoimmune diseases. Participants will undergo tests to check for CTEPH and will be monitored throughout the study. The trial is not yet recruiting, so it’s a good idea to stay informed about when it will begin if you think you might qualify.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 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:
- • 1. 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
- 2. 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 Criteria:
- • Not agreeing to participate in the project
- • Contraindications to treatment
About Institute Of Health Information And Statistics Of The Czech Republic
The Institute of Health Information and Statistics of the Czech Republic (IHIS CR) is a pivotal organization dedicated to enhancing public health through the systematic collection, analysis, and dissemination of health-related data. As a key sponsor of clinical trials, IHIS CR plays a crucial role in supporting evidence-based healthcare decision-making by providing valuable insights into health trends, outcomes, and resource allocation. With a commitment to fostering collaboration among healthcare providers, researchers, and policymakers, the institute aims to improve health services and outcomes across the Czech Republic, ultimately contributing to the advancement of national and international health initiatives.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Pavel Jansa, prof.
Study Director
General University Hospital of Prague
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported