Assessment of Airway Obstruction in Infants With Lower Respiratory Infections
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| ClinicalTrials.gov Identifier: NCT00435994 |
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Recruitment Status :
Completed
First Posted : February 16, 2007
Results First Posted : June 1, 2016
Last Update Posted : June 1, 2016
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Bronchiolitis Respiratory Syncytial Virus Infections | Drug: Inhaled primatene will be given as a breathing treatment Other: Nasal Washing | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 59 participants |
| Allocation: | Non-Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Assessment of Airway Obstruction in Infants With Lower Respiratory Infections |
| Study Start Date : | December 2003 |
| Actual Primary Completion Date : | March 2009 |
| Actual Study Completion Date : | December 2012 |
| Arm | Intervention/treatment |
|---|---|
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Infants with viral lower respiratory infections
Infants between the ages of 2-24 month, with viral lower respiratory infection defined as first episode of wheezing and shortness of breath preceded by an upper respiratory tract infection, including hospitalized infants
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Drug: Inhaled primatene will be given as a breathing treatment
While the research subject is sedated an inhaled mist of primatene mist will be given to the patient.
Other Name: epinephrine 0.5ml of the 2.25% concentration Other: Nasal Washing 1-3 mls of normal saline will be instilled into the infant's nose and then aspirated to obtain the nasal fluid, which will be analyzed for VEGF level by ELISA and viral antigens by immunoflourescence |
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Healthy Control
Healthy infants between the ages of 2-24 month
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Drug: Inhaled primatene will be given as a breathing treatment
While the research subject is sedated an inhaled mist of primatene mist will be given to the patient.
Other Name: epinephrine 0.5ml of the 2.25% concentration Other: Nasal Washing 1-3 mls of normal saline will be instilled into the infant's nose and then aspirated to obtain the nasal fluid, which will be analyzed for VEGF level by ELISA and viral antigens by immunoflourescence |
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Bronchiolitis-Nasal wash only
Infants 2 months to 24 months who were diagnosed with bronchiolitis received nasal wash only
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Other: Nasal Washing
1-3 mls of normal saline will be instilled into the infant's nose and then aspirated to obtain the nasal fluid, which will be analyzed for VEGF level by ELISA and viral antigens by immunoflourescence |
- Lung Function [ Time Frame: Baseline, Post bronchodilator (up to 10 minutes, Post-epinephrine (up to 30 minutes) ]Lung functions were obtained under sedation using Chloral Hydrate. Forced expiratory flows are a lung volume at which the airway pressure is equal to 30 cm H2O (V30). Forced expiratory flows are measured at 75% FVC (FEF75). Measurements were repeated post bronchodilator and again post Epinephrine. A higher Z-score reflects better lung function.
- Endothelial Growth Factor (VEGF) [ Time Frame: During nasal wash ]Analysis for VEGF level by ELISA
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| Ages Eligible for Study: | 2 Months to 2 Years (Child) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Group 1 Infants between 2 and 24 months that are healthy
- Group 2 Infants between 2 and 24 months that have RSV or bronchiolitis and defined as the first episode of wheezing
Exclusion Criteria:
- Group 1 and 2 - no cardiac disease, no oxygen requirement, prematurity < 37 weeks, and cannot be in the ICU.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00435994
| United States, Indiana | |
| Riley Hospital for Children | |
| Indianapolis, Indiana, United States, 46202 | |
| Principal Investigator: | Robert S. Tepper, MD | Indiana University |
| Responsible Party: | Indiana University School of Medicine |
| ClinicalTrials.gov Identifier: | NCT00435994 |
| Other Study ID Numbers: |
0311-21 |
| First Posted: | February 16, 2007 Key Record Dates |
| Results First Posted: | June 1, 2016 |
| Last Update Posted: | June 1, 2016 |
| Last Verified: | May 2016 |
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Infant Respiratory Syncytial Virus Bronchiolitis |
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Infections Communicable Diseases Bronchiolitis Respiratory Tract Infections Respiratory Syncytial Virus Infections Airway Obstruction Disease Attributes Pathologic Processes Virus Diseases Bronchitis Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases Respiratory Insufficiency |
Respiration Disorders Pneumovirus Infections Paramyxoviridae Infections Mononegavirales Infections RNA Virus Infections Epinephrine Adrenergic alpha-Agonists Adrenergic Agonists Adrenergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Adrenergic beta-Agonists Bronchodilator Agents Autonomic Agents |

