SARS Clinical Trial
NCT number | NCT00173459 |
Other study ID # | 9461700671 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | September 12, 2005 |
Last updated | September 12, 2005 |
Verified date | July 2004 |
Source | National Taiwan University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Taiwan: Department of Health |
Study type | Observational |
Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel coronavirus (SARS-CoV). The major clinical features of SARS include fever, dyspnea, lymphopenia, and a rapid progression of pulmonary infiltrates on chest radiologic images. The SARS-related deaths have resulted mainly from pulmonary complications, including progressive respiratory failure due to alveolar damage and acute respiratory distress syndrome (ARDS). Pathological changes in SARS suggest that SARS sequelae such as infiltration of PMN in lung tissue, multiple organ dysfunction and ARDS have been associated with cytokines and chemokine dysregulation. Some patients still manifested lung injury at a time when the viral load was falling also supports the immune nature of the lung damage. We therefore undertook an analysis of dynamic production of cytokine/chemokines in SARS patients with an initial normal chest radiograph in order to improve understanding of disease pathogenesis and improve patient management.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | 20 Years and older |
Eligibility |
Inclusion Criteria: - SARS group: Patients with SARS Exclusion Criteria: - Hospital acquired pneumonia |
Observational Model: Case Control, Time Perspective: Longitudinal
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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National Taiwan University Hospital |
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