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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01090557 |
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Date of registration:
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06/10/2009 |
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Primary sponsor: |
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Public title:
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Exhaled Nitric Oxide in Respiratory Syncytial Virus (RSV) Bronchiolitis: a Pilot Study
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Scientific title:
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A Prospective, Pilot Study Measuring Exhaled Nitric Oxide Levels in Infants and Young Children Admitted to the Hospital for Respiratory Syncytial Virus (RSV) or Other Viral Lower Respiratory Tract Infections |
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Date of first enrolment:
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October 2007 |
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Target sample size:
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60 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01090557 |
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Study type:
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Observational |
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Study design:
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Observational Model: Case Control, Time Perspective: Prospective
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Countries of recruitment
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United States
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Contacts
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Name:
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Maria L Quintos-Alagheband, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Winthrop University Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Admitted subjects with diagnosis of bronchiolitis, viral pneumonia or other
significant respiratory viral infection
Exclusion Criteria:
- asthma/RAD
- recurrent wheezing
- "recurrent bronchiolitis"
- allergic rhinitis
- atopy
- chronic lung disease
- hypertension
- heart failure
- pulmonary hypertension
- primary ciliary dyskinesia
- bronchiectasis
- alveolitis
- lung transplant rejection
- pulmonary sarcoidosis
- chronic cough (i.e. greater four weeks)
- systemic sclerosis
- hypersensitivity
- cystic fibrosis
- HIV
- sickle cell anemia
- cardiac pulmonary bypass
- liver cirrhosis
- alpha-1 anti-trypsin disease
- interstitial lung
Age minimum:
N/A
Age maximum:
4 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Bronchiolitis
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RSV Infection
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Intervention(s)
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Other: Collection of exhaled breath
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Primary Outcome(s)
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Difference in feNO level between RSV and non-RSV infection in hospitalized pediatric patients with viral lower respiratory illness as well as with control subjects
[Time Frame: 2 years]
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Secondary Outcome(s)
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FeNO levels correlate with the severity of respiratory symptoms in children with acute viral respiratory illness
[Time Frame: 2 years]
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FeNO levels in viral respiratory illness will vary with steroid use
[Time Frame: 2 years]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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