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Investigating Severe Acute Respiratory Syndrome (SARS) - Article


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Severe Acute Respiratory Syndrome (SARS)

Sars; Sars/severe Acute Respiratory Syndrome; Severe Acute Respiratory Syndrome


Clinical Trial: Investigating Severe Acute Respiratory Syndrome (SARS)

This study is currently recruiting patients.

Sponsored by: National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by: Warren G Magnuson Clinical Center (CC)

Purpose

Severe Acute Respiratory Syndrome (SARS) is a newly recognized illness that can be fatal.

The purpose of this study is to better understand SARS by collecting samples of blood and other body fluids of people who have been exposed to SARS or who are suspected to have the illness.

Up to 300 volunteers aged 18 years or older will be enrolled in this study. Participants will donate blood samples and, if appropriate, samples of fluid from the lungs, nose, or throat. Researchers will test these samples for proteins that control or mediate inflammatory or immune responses. The patterns of these proteins will reveal how SARS affects the body and the efforts the body makes to fight off the infection.

Condition
SARS Virus

MedlinePlus consumer health information 

Study Type: Observational
Study Design: Natural History

Official Title: An Investigation of the Inflammatory Response in Severe Acute Respiratory Syndrome (SARS)

Further Study Details: 

Expected Total Enrollment:  400

Study start: August 4, 2003

Severe acute respiratory syndrome (SARS) is a newly recognized illness associated with substantial mobidity and mortality. Patients develop fever followed by rapidly progressive and even fatal respiratory disease. SARS is associated with infection with a novel coronavirus. The evaluation of the inflammatory responses evoked by SARS may yield information regarding its pathogenesis and help with patient management. This protocol, then, merely aims to study disease pathogenesis and natural history, by studying samples and data that are collected by outside physicians or physicians at the Clinical Center and sent for evaluation of the inflammatory response.

Eligibility

Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

INCLUSION CRITERIA - CASES:
Patients fulfilling the CDC case definition or WHO definition for suspected or probable SARS.
Newly identified patients found to have recovered from SARS can also be enrolled.
EXCLUSION CRITERIA - CASES:
Patients diagnoses with alternative illnesses as the cause of the symptoms.
INCLUSION CRITERIA - HEALTHY VOLUNTEERS:
For the purpose of this study, a healthy volunteer is defined as a healthy male or female, age 18 and above.
Volunteers will be excluded if they have a pre-existing or concurrent serious chronic medical or psychiatric illness.
Chronic medication use will be evaluated on a case-by-case basis.
They will also be excluded if they have received an investigational drug in the past 3 months.

Location and Contact Information


Maryland
      National Institute of Allergy and Infectious Diseases (NIAID), 9000 Rockville Pike,  Bethesda,  Maryland,  20892,  United States; Recruiting
Patient Recruitment and Public Liaison Office  1-800-411-1222    prpl@mail.cc.nih.gov 
TTY  1-866-411-1010 

More Information

Detailed Web Page

Study ID Numbers:  030240; 03-I-0240
Record last reviewed:  July 9, 2004
Last Updated:  November 23, 2004
Record first received:  August 5, 2003
ClinicalTrials.gov Identifier:  NCT00066209
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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October 6, 2008



Page Updated: October 3, 2005
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