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Efficacy of Nebulised Beclometasone in Viral Wheezing Prophylaxis (ENBe)

Primary Purpose

Bronchial Spasm, Respiratory Sounds, Respiratory Tract Infections

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Beclomethasone
Placebo
Sponsored by
Mario Negri Institute for Pharmacological Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Bronchial Spasm focused on measuring Bronchial Spasm, Respiratory Tract Infections, Viral wheezing, Child, Preschool, Beclomethasone, Italy, Physicians, Primary Care, Pediatrics

Eligibility Criteria

12 Months - 71 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Outpatient children 1-5 years old
  • Presence of any viral upper respiratory tract infection symptoms
  • At least one episode of viral wheezing (diagnosed by a physician) in the last 12 months.
  • No, or minimal, asthma-like symptoms in between separate airway infections

Exclusion Criteria:

  • Steroid hypersensitivity
  • Inhaled and/or oral corticosteroid use in the preceding month
  • Chronic respiratory disease (e.g. cystic fibrosis, broncho-pulmonary dysplasia)
  • Presence of wheezing at the entry visit

Sites / Locations

  • ASL NA/3 Sud
  • AUSL Chieti
  • ASL Monza Brianza
  • ASL Torino 3
  • ASP di Reggio Calabria
  • Ausl Roma E
  • AUSL Taranto
  • Azienda ULSS 20 Verona
  • ASL 12

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Beclomethasone

Arm Description

Beclometasone suspension 400 mcg will be administered through a nebuliser twice a day, in the morning and in the evening, for 10 days

Outcomes

Primary Outcome Measures

% of children with wheezing (diagnosed by the paediatrician) during the URTI episode.

Secondary Outcome Measures

% of patients needing medical care during the treatment period;
% of patients receiving rescue medication during the treatment period;
% of patients admitted to an emergency department during the treatment period
Duration of the respiratory tract infection episode
% of patients with an asthma-like symptom score (rated by parents) >= 7
Mean asthma-like symptom score for each child
Time to the first viral wheezing episode after the end of the treatment
Frequency of respiratory tract infection episodes during the 6 month follow-up period
Frequency of viral wheezing episodes during the 6 month follow-up period
% of parents who consider the treatment helpful
% of patients fully adherent to therapy
average cost per patient

Full Information

First Posted
December 22, 2010
Last Updated
March 10, 2014
Sponsor
Mario Negri Institute for Pharmacological Research
Collaborators
Agenzia Italiana del Farmaco, Associazione Culturale Pediatri
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1. Study Identification

Unique Protocol Identification Number
NCT01265342
Brief Title
Efficacy of Nebulised Beclometasone in Viral Wheezing Prophylaxis
Acronym
ENBe
Official Title
Efficacy Of Nebulised Beclometasone Versus Placebo In Preventing Viral Wheezing In Pre-School Children
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
October 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mario Negri Institute for Pharmacological Research
Collaborators
Agenzia Italiana del Farmaco, Associazione Culturale Pediatri

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Inhaled steroids, in particular beclomethasone, are widely prescribed in Italy as symptomatic treatment of upper respiratory infections without evidence of efficacy. The purpose of this study is to evaluate the efficacy of beclomethasone (administered by nebuliser twice a day) in preventing viral wheezing in pre-school children who had had episodes in the preceding 12 months.
Detailed Description
Viral wheezing (intermittent episodes of wheezing induced by viral infection of the upper respiratory tract) is a common condition in pre-school children. Its incidence is estimated between 6 and 30% and varies depending on criteria, diagnosis, and age definition used. Viral wheezing, however, is different from atopic asthma, since in 60% of cases symptoms disappear before the age of 6 . The efficacy of drug treatments in the prevention and/or treatment of viral wheezing is controversial; short acting beta 2 agonists are often considered first choice therapies even if evidence is scarce The usefulness of inhaled steroids is also debated: no benefits are documented for maintenance with low dose inhaled corticosteroids, while their episodic use at a high dose may have a modest improvement in symptoms. Despite the scant evidence, however, nebulised steroids in particular beclomethasone, are widely prescribed in Italy as prophylaxis or treatment for viral wheezing. Beclometasone is the third most prescribed drug in Italian children, with a prevalence estimated around 15% A randomized placebo-controlled trial was therefore planned to evaluate the effectiveness of nebulised beclometasone in preventing viral wheezing in children with upper respiratory tract infections. Besides investigating the drug efficacy, the study could also monitor the incidence of viral wheezing recurrence in preschool children, the disease's natural history and the different therapeutic approaches used by the physicians. The study will involve 36 Italian family paediatricians from 9 local health units. Children will be randomized to receive beclomethasone or placebo. The treatment period will last 10 days, and it will be followed by an observational 6 month follow-up period. Three visits are scheduled: the first at baseline, the second at the end of the treatment period and the third at the end of follow-up period. During the 10 day treatment period, symptoms will be recorded by the parents on a diary. A clinical evaluation will be performed by the paediatrician during the entry visit and at the end of the treatment period. Moreover, parents will be requested to contact the paediatrician if wheezing occurs during the treatment period and/or the child does not improve within 72 hours from the start of the therapy. In case of wheezing and/or lack of improvement, paediatricians should visit the child, evaluate the presence of wheezing and rate it. A wheeze score will be assigned as follows: 0 = no wheezing, 1 = end-expiratory wheeze only, 2 = wheeze during entire expiratory with or without inspiratory phase, audible with stethoscope only, 3 = inspiratory and expiratory wheezing audible without stethoscope.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchial Spasm, Respiratory Sounds, Respiratory Tract Infections
Keywords
Bronchial Spasm, Respiratory Tract Infections, Viral wheezing, Child, Preschool, Beclomethasone, Italy, Physicians, Primary Care, Pediatrics

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
576 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Beclomethasone
Arm Type
Experimental
Arm Description
Beclometasone suspension 400 mcg will be administered through a nebuliser twice a day, in the morning and in the evening, for 10 days
Intervention Type
Drug
Intervention Name(s)
Beclomethasone
Intervention Description
Beclomethasone nebulised suspension 400 micrograms twice a day for 10 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo nebulised suspension twice a day for 10 days
Primary Outcome Measure Information:
Title
% of children with wheezing (diagnosed by the paediatrician) during the URTI episode.
Secondary Outcome Measure Information:
Title
% of patients needing medical care during the treatment period;
Title
% of patients receiving rescue medication during the treatment period;
Title
% of patients admitted to an emergency department during the treatment period
Title
Duration of the respiratory tract infection episode
Title
% of patients with an asthma-like symptom score (rated by parents) >= 7
Title
Mean asthma-like symptom score for each child
Title
Time to the first viral wheezing episode after the end of the treatment
Title
Frequency of respiratory tract infection episodes during the 6 month follow-up period
Title
Frequency of viral wheezing episodes during the 6 month follow-up period
Title
% of parents who consider the treatment helpful
Title
% of patients fully adherent to therapy
Title
average cost per patient

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Months
Maximum Age & Unit of Time
71 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Outpatient children 1-5 years old Presence of any viral upper respiratory tract infection symptoms At least one episode of viral wheezing (diagnosed by a physician) in the last 12 months. No, or minimal, asthma-like symptoms in between separate airway infections Exclusion Criteria: Steroid hypersensitivity Inhaled and/or oral corticosteroid use in the preceding month Chronic respiratory disease (e.g. cystic fibrosis, broncho-pulmonary dysplasia) Presence of wheezing at the entry visit
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antonio Clavenna, MD
Organizational Affiliation
Mario Negri Institute for Pharmacological Research, Milan, Italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
ASL NA/3 Sud
City
Castellammare di Stabia
Country
Italy
Facility Name
AUSL Chieti
City
Chieti
Country
Italy
Facility Name
ASL Monza Brianza
City
Monza
Country
Italy
Facility Name
ASL Torino 3
City
Pinerolo
Country
Italy
Facility Name
ASP di Reggio Calabria
City
Reggio Calabria
Country
Italy
Facility Name
Ausl Roma E
City
Roma
Country
Italy
Facility Name
AUSL Taranto
City
Taranto
Country
Italy
Facility Name
Azienda ULSS 20 Verona
City
Verona
Country
Italy
Facility Name
ASL 12
City
Viareggio
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
24534400
Citation
Clavenna A, Sequi M, Cartabia M, Fortinguerra F, Borghi M, Bonati M; ENBe Study Group. Effectiveness of nebulized beclomethasone in preventing viral wheezing: an RCT. Pediatrics. 2014 Mar;133(3):e505-12. doi: 10.1542/peds.2013-2404. Epub 2014 Feb 17.
Results Reference
result

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Efficacy of Nebulised Beclometasone in Viral Wheezing Prophylaxis

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