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Acoustic Assessment of Nebulized Epinephrine Versus Albuterol for RSV Bronchiolitis- a Double Blind Study
This study has been terminated.
First Received: August 6, 2006   No Changes Posted
Sponsor: Rambam Health Care Campus
Information provided by: Rambam Health Care Campus
ClinicalTrials.gov Identifier: NCT00361452
  Purpose

Bronchiolitis is a common disease of infancy and a main reason for infants' hospital admissions in the first 2 years of life. The main cause of bronchiolitis is RSV (respiratory syncytial virus). Though, Treatment is mainly supportive, the treatment benefit of nebulized epinephrine or albuterol has been largely debated for the past years. Most of the clinical studies used clinical parameters to detect and compare the effectiveness of such medical interventions. In this study we will use non invasive computerized method of wheeze and crackles quantification to compare the effectiveness of nebulized epinephrine vs albuterol in RSV Bronchiolitis.


Condition Intervention Phase
Rsv Bronchiolitis
Drug: nebulized epinephrine and nebulized albuterol
Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study
Official Title: Acoustic Assessment of Nebulized Epinephrine Versus Albuterol for RSV Bronchiolitis- a Double Blind Study

Resource links provided by NLM:


Further study details as provided by Rambam Health Care Campus:

Primary Outcome Measures:
  • respiratory clinical score
  • computerized quantification of wheezing and crackles

Estimated Enrollment: 30
Study Start Date: December 2000
Estimated Study Completion Date: May 2001
Detailed Description:

Inpatient Infants younger than 2 years of age with first episode of RSV bronchiolitis will be randomly assigned to treatment with nebulized epinephrine (1 mg diluted with 3 ml of 0.9% saline) or nebulized albuterol (2.5 mg diluted with 3.5 ml of 0.9% saline). Both solutions will be provided in identical containers.

Clinical assessment and clinical score will be done before treatment, 10 and 30 minutes after treatment. The following parameters were recorded at each time point, wheezing, respiratory distress, O2 saturation, respiratory rate and heart rate. Computerized lung sounds as well, will be recorded before treatment, 10 and 30 minutes after treatment via 4 contact sensors attached to the chest.

  Eligibility

Ages Eligible for Study:   up to 1 Year
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Under one year of age
  • first episode of wheezing and dyspnea
  • RSV antigen detected by ELISA
  • parents signed informed consent.

Exclusion Criteria:

  • infants with chronic lung disease
  • cardiac disease
  • other chronic conditions.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00361452

Locations
Israel
Pediatric Ward, Rambam Medical Centre
HAIFA, Israel, 31096
Sponsors and Collaborators
Rambam Health Care Campus
Investigators
Principal Investigator: LEA BENTUR, MD Rambam medical centre, pediatric pulmonary unit, HAIFA
  More Information

No publications provided by Rambam Health Care Campus

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Study ID Numbers: epinephrine_albuterol_rsv.ctil
Study First Received: August 6, 2006
Last Updated: August 6, 2006
ClinicalTrials.gov Identifier: NCT00361452     History of Changes
Health Authority: Israel: Ethics Commission

Additional relevant MeSH terms:
Respiratory System Agents
Neurotransmitter Agents
Bronchial Diseases
Adrenergic Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Albuterol
Reproductive Control Agents
Adrenergic Agonists
Lung Diseases, Obstructive
Tocolytic Agents
Respiratory Tract Infections
Respiratory Tract Diseases
Therapeutic Uses
Vasoconstrictor Agents
Bronchitis
Epinephrine
Adrenergic alpha-Agonists
Adrenergic beta-Agonists
Sympathomimetics
Bronchiolitis
Anti-Asthmatic Agents
Cardiovascular Agents
Pharmacologic Actions
Mydriatics
Autonomic Agents
Lung Diseases
Peripheral Nervous System Agents
Bronchodilator Agents

ClinicalTrials.gov processed this record on November 27, 2009