The Interaction Between Severe Acute Respiratory Distress Syndrome Viral Proteins and Monocytes

This study has been withdrawn prior to enrollment.
Sponsor:
Information provided by:
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT00172263
First received: September 12, 2005
Last updated: December 6, 2012
Last verified: December 2012

September 12, 2005
December 6, 2012
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Complete list of historical versions of study NCT00172263 on ClinicalTrials.gov Archive Site
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The Interaction Between Severe Acute Respiratory Distress Syndrome Viral Proteins and Monocytes
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Severe acute respiratory syndrome (SARS) is a new threat to public health since November, 2002. The SARS is highly contagious and is believed to be transmitted by person-to-person through droplet and direct contact. The patients present with fever, chills, cough, myalgia, dyspnea, and diarrhea. The symptoms aggravate in the second week and nearly 40% of the patients develop respiratory failure that requires assisted ventilation. The mortality rate is reported as 6.5%-7%.

After several months, the world scientists found the etiology to be a new coronavirus not belonging to the previous coronavirus group I, II and III. The new virus is called SARS associated coronavirus (SARS-CoV).

Although the high morbidity and mortality of SARS occurred in adults, there was rare mortality reported in the children. The report from Hong Kong pointed out that the symptoms of SARS in younger children were milder and the clinical course was not as aggressive as in adults. Therefore, the aim of the project is to design the experiment to see the differences of immunological responses to SARS-CoV protein in healthy younger children, teenagers, and adults. The investigators hope that the result could explain the reason for milder disease in younger children and the immunological pathogenesis of SARS.

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Interventional
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Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Severe Acute Respiratory Syndrome
Procedure: blood sampling
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
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Inclusion Criteria:

  • Healthy adults, children and cord blood
Both
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Yes
Contact information is only displayed when the study is recruiting subjects
China
 
NCT00172263
9261701054
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National Taiwan University Hospital
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Principal Investigator: Li-Chieh Wang, MD National Taiwan University Hospital
National Taiwan University Hospital
December 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP