Pulmonary Hypertension Screening for Rheumatology Patients (SOPHIE)
NCT03446339 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1800
Last updated 2021-08-03
Summary
Pulmonary arterial hypertension (PAH) is a serious and often fatal complication of connective tissue diseases including systemic sclerosis and systemic lupus erythematosus. It has been reported primarily from European series that the prevalence of PAH in patients with connective tissue diseases particularly systemic sclerosis is as high as 15-20%. However, given the paucity of medical literature in the area from Chinese population, the prevalence of PAH amongst Chinese patients with these conditions is largely unknown. Even worse, PAH is often undiagnosed amongst patients with connective tissue diseases due to the lack of awareness and/or access to echocardiography, which is a non-invasive first-line screening tool for PAH. As a result, most patients at diagnosis of PAH are at a relatively late stage, rendering pharmacological treatment less effective. Here, the investigators propose a territory-wide pulmonary hypertension screening for patients with connective tissue disease in order to (1) detect pulmonary hypertension amongst patients with connective tissue disease through systematic screening, and (2) understand the prevalence of pulmonary hypertension in Chinese patients with connective tissue diseases.
Conditions
- Connective Tissue Diseases
- Systemic Sclerosis
- Systemic Lupus Erythematosus
Sponsors & Collaborators
-
The University of Hong Kong
lead OTHER
Principal Investigators
-
David Chung-Wah Siu, Professor · The Universtiy of Hong Kong
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-08-03
- Primary Completion
- 2023-08-31
- Completion
- 2023-12-31
Countries
- China
Study Locations
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