Prevalence of Pulmonary Hypertension (PAH) in Patients With Thalassemia
NCT01496963 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1500
Last updated 2022-08-04
Summary
This is a multicenter observational case-control analysis lasting 12 months aimed at determining the prevalence of pulmonary hypertension (PAH) in patients with Thalassemia Major and Intermedia. The patients will be followed, treated and examined according to the best standard clinical practice dictated by the Italian Society for the study of Hemoglobinopathies (SITE), Thalassemia International Federation (TIF)and the Task Force for Diagnosis and Treatment of Pulmonary Hypertension of European Society of Cardiology (ESC); European Respiratory Society (ERS); International Society of Heart and Lung Transplantation (ISHLT) guidelines.
Conditions
- Thalassemia Major
- Thalassemia Intermedia
- Pulmonary Arterial Hypertension
Interventions
- OTHER
-
Physician standard-of-care according to ESC/ERS Guidelines
Physician standard-of-care
Sponsors & Collaborators
-
Ente Ospedaliero Ospedali Galliera
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-01-31
- Primary Completion
- 2021-12-31
- Completion
- 2021-12-31
Countries
- Italy
Study Locations
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