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| Sponsor: | University Hospitals of Cleveland |
|---|---|
| Information provided by: | University Hospitals of Cleveland |
| ClinicalTrials.gov Identifier: | NCT00798616 |
Purpose
The purpose of the study is to determine whether corticosteroids are beneficial to children with bronchiolitis whose breathing gets better after being given a breathing treatment with albuterol.
| Condition | Intervention |
|---|---|
|
Bronchiolitis |
Drug: prednisolone or methylprednisolone Drug: placebo |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Are Steroids Efficacious in Hospitalized Patients With Bronchiolitis Who Show an Objective Clinical Improvement After Albuterol ("Albuterol Responders")? |
| Enrollment: | 0 |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: Responders/Placebo
Albuterol responders being given placebo
|
Drug: placebo
oral or IV placebo
|
|
Active Comparator: Responders/Steroids
albuterol responders being given steroids
|
Drug: prednisolone or methylprednisolone
either prednisolone 2mg/kg PO once daily or methylprednisolone 1.6mg/kg IV once daily (if IV access is present) for length of hospitalization, for a maximum of seven days
Other Names:
|
|
Placebo Comparator: Non-responders/placebo
non-albuterol responders being given placebo
|
Drug: placebo
oral or IV placebo
|
|
Active Comparator: non-responders/steroids
non-albuterol responders being given steroids
|
Drug: prednisolone or methylprednisolone
either prednisolone 2mg/kg PO once daily or methylprednisolone 1.6mg/kg IV once daily (if IV access is present) for length of hospitalization, for a maximum of seven days
Other Names:
|
Eligibility| Ages Eligible for Study: | up to 24 Months |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Ohio | |
| University Hospitals of Cleveland | |
| Cleveland, Ohio, United States, 44106 | |
| Principal Investigator: | Steven L Shein, MD | University Hospitals of Cleveland |
More Information
| Responsible Party: | Steven Shein, Chief Resident, Department of Pediatrics, University Hospitals of Cleveland |
| ClinicalTrials.gov Identifier: | NCT00798616 History of Changes |
| Other Study ID Numbers: | UHC 07-08-36 |
| Study First Received: | November 25, 2008 |
| Last Updated: | September 22, 2011 |
| Health Authority: | United States: Institutional Review Board |
|
bronchiolitis steroids corticosteroids albuterol |
child infant pediatric |
|
Bronchiolitis Bronchitis Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases Respiratory Tract Infections Albuterol Methylprednisolone Methylprednisolone acetate Prednisolone acetate Prednisolone Methylprednisolone Hemisuccinate Prednisolone phosphate Tocolytic Agents |
Reproductive Control Agents Physiological Effects of Drugs Pharmacologic Actions Therapeutic Uses Adrenergic beta-2 Receptor Agonists Adrenergic beta-Agonists Adrenergic Agonists Adrenergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Bronchodilator Agents Autonomic Agents Peripheral Nervous System Agents Anti-Asthmatic Agents Respiratory System Agents |