search
Back to results

Effect of OM-85 BV on Wheezing Related Morbidity in Children With Recurrent Wheezing

Primary Purpose

Asthma

Status
Completed
Phase
Phase 4
Locations
Turkey
Study Type
Interventional
Intervention
OM-85 BV (Broncho-Vaxom)
OM-85 BV (placebo)
Sponsored by
Kecioren Education and Training Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Asthma focused on measuring wheezing, asthma, childhood, OM-85 BV, Broncho-Vaxom

Eligibility Criteria

6 Months - 6 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children with recurrent wheezing who had at least 3 wheezing attacks in the last 6 months
  • Children with asthma who had at least 3 wheezing attacks in the last 6 months

Exclusion Criteria:

  • Chronic lung disease
  • Immun deficiency
  • Malabsorption
  • Anatomic abnormalities of the respiratory tract
  • Gastroesophageal reflux disease

Sites / Locations

  • Kecioren Education and Training Hospital
  • Keçiören Education and Training Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

1 Broncho-Vaxom

2 (Placebo OM-85 BV)

Arm Description

The children received one capsule per oral, OM-85 BV (3.5 mg) per day for the first 10 consecutive days of each month for 3 consecutive months.

The children received one capsule per oral, placebo per day for the first 10 consecutive days of each month for 3 consecutive months.

Outcomes

Primary Outcome Measures

Mean Rate of Wheezing Attacks
Acute wheezing attack was defined as episode of progressive increase in shortness of breath, cough, wheezing, retraction of the chest and chest tightness, or combination of these symptoms. When wheezing attack occured it was Over the 12 months of the study mean number (rate) of wheezing attacks/per patient was calculated and compared with placebo. This outcome measure was calculated by dividing cumulative wheezing attacks to number of participants in each group.

Secondary Outcome Measures

Mean Duration (in Day) of Wheezing Attacks Per Patient
Over the 12 months of the study we calculated mean duration of each wheezing attacks/per patients.This measure was calculated separately for each participants by dividing duration of wheezing attacks to number of wheezing attacks.
Number of Common Cold
All the common colds were recorded during the 12 months of the study. At the and of the study period the two groups were compared according to the number of common-cold/per patient over the 12 months of the trial. This outcome was calculated by dividing cumulative number of common colds by number of participants in each group over the 12 months of the trial.
Number of Wheezing Attacks That Required Systemic Steroid Therapy
All the wheezing attacks which were enough severe to require systemic steroid therapy were recorded over the 12 months of the study. At the and of the study period, number of wheezing attacks that required systemic steroid therapy/per patients were calculated. This outcome was calculated by dividing cumulative number of wheezing attacks that required systemic steroid therapy by number of participants in each group.
Number of Hospitalizations
During the study period of 12 months all hospitalizations for wheezing attacks were recorded. Over the 12 months of the trial mean number of hospitalizations/per patients were calculated. This outcome was calculated by dividing cumulative number of hospitalizations by number of participants in each group over the 12 months of the trial.
Duration of Hospitalization/Per Patient
Over the 12 months of the study we calculated mean duration of hospitalization/per patients.
Effect of OM-85 BV on Cytokine Levels
Cytokine levels were not measured during the trial because of unavailability of laboratory resources.

Full Information

First Posted
August 11, 2008
Last Updated
July 4, 2014
Sponsor
Kecioren Education and Training Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT00733226
Brief Title
Effect of OM-85 BV on Wheezing Related Morbidity in Children With Recurrent Wheezing
Official Title
Phase IV Study of Effect of OM-85 BV (Broncho-Vaxom) on Wheezing Related Morbidity in Children With Recurrent Wheezing
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
October 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kecioren Education and Training Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether OM-85 BV (Broncho-Vaxom)has any effect on respiratory infections, infection related wheezing attacks, beta-2 agonist use, duration of attacks and effect on serum cytokine levels.
Detailed Description
Context: Respiratory infections are the major cause of wheezing attacks in children with recurrent wheezing or asthma in preschool age. OM-85 BV is an bacteria lysate which has been proven to prevent respiratory infections about 40 percent in children. Objective: To determine if using OM-85 BV diminish the number and duration of the respiratory infections and respiratory infection related wheezing attacks,beta-2 agonist and steroid use, and number and duration of hospitalizations in children with recurrent wheezing and asthma. And also to determine if OM-85 BV has any effect on serum cytokine levels after 6 months. Study Design/Setting/Participants: A double-blind, randomized, controlled trial of OM-85 BV versus placebo for children 6 months to 6 years of age who have respiratory tract infection related recurrent wheezing attacks. Intervention: Participants will receive either active Broncho-Vaxom or placebo for 3 months. Study Measures: They follow up for 1 year for number and duration of wheezing attacks, number, type and duration of respiratory infections, number and duration of beta-2 agonist use, number and duration of steroid use and number and duration of hospitalizations. Serum cytokine levels will measure to determine if Broncho-Vaxom has any effect on serum cytokine levels (at the beginning of the trial and sixth months of the trial).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
wheezing, asthma, childhood, OM-85 BV, Broncho-Vaxom

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1 Broncho-Vaxom
Arm Type
Active Comparator
Arm Description
The children received one capsule per oral, OM-85 BV (3.5 mg) per day for the first 10 consecutive days of each month for 3 consecutive months.
Arm Title
2 (Placebo OM-85 BV)
Arm Type
Placebo Comparator
Arm Description
The children received one capsule per oral, placebo per day for the first 10 consecutive days of each month for 3 consecutive months.
Intervention Type
Drug
Intervention Name(s)
OM-85 BV (Broncho-Vaxom)
Other Intervention Name(s)
Bronchovaxom 3.5 mg capsule
Intervention Description
3.5 mg capsule, 1 capsule per day for first 10 day of the month, for 3 months
Intervention Type
Drug
Intervention Name(s)
OM-85 BV (placebo)
Other Intervention Name(s)
Bronchovaxom 3.5 mg placebo capsule
Intervention Description
3.5 mg oral placebo capsule, 1 placebo capsule per day for first 10 days of the months for 3 months
Primary Outcome Measure Information:
Title
Mean Rate of Wheezing Attacks
Description
Acute wheezing attack was defined as episode of progressive increase in shortness of breath, cough, wheezing, retraction of the chest and chest tightness, or combination of these symptoms. When wheezing attack occured it was Over the 12 months of the study mean number (rate) of wheezing attacks/per patient was calculated and compared with placebo. This outcome measure was calculated by dividing cumulative wheezing attacks to number of participants in each group.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Mean Duration (in Day) of Wheezing Attacks Per Patient
Description
Over the 12 months of the study we calculated mean duration of each wheezing attacks/per patients.This measure was calculated separately for each participants by dividing duration of wheezing attacks to number of wheezing attacks.
Time Frame
12 months
Title
Number of Common Cold
Description
All the common colds were recorded during the 12 months of the study. At the and of the study period the two groups were compared according to the number of common-cold/per patient over the 12 months of the trial. This outcome was calculated by dividing cumulative number of common colds by number of participants in each group over the 12 months of the trial.
Time Frame
12 months
Title
Number of Wheezing Attacks That Required Systemic Steroid Therapy
Description
All the wheezing attacks which were enough severe to require systemic steroid therapy were recorded over the 12 months of the study. At the and of the study period, number of wheezing attacks that required systemic steroid therapy/per patients were calculated. This outcome was calculated by dividing cumulative number of wheezing attacks that required systemic steroid therapy by number of participants in each group.
Time Frame
12 months
Title
Number of Hospitalizations
Description
During the study period of 12 months all hospitalizations for wheezing attacks were recorded. Over the 12 months of the trial mean number of hospitalizations/per patients were calculated. This outcome was calculated by dividing cumulative number of hospitalizations by number of participants in each group over the 12 months of the trial.
Time Frame
12 months
Title
Duration of Hospitalization/Per Patient
Description
Over the 12 months of the study we calculated mean duration of hospitalization/per patients.
Time Frame
12 months
Title
Effect of OM-85 BV on Cytokine Levels
Description
Cytokine levels were not measured during the trial because of unavailability of laboratory resources.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children with recurrent wheezing who had at least 3 wheezing attacks in the last 6 months Children with asthma who had at least 3 wheezing attacks in the last 6 months Exclusion Criteria: Chronic lung disease Immun deficiency Malabsorption Anatomic abnormalities of the respiratory tract Gastroesophageal reflux disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
C H RAZI, MD
Organizational Affiliation
Kecioren Education and Training Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
C H Razi, MD
Organizational Affiliation
Kecioren Education and Training Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kecioren Education and Training Hospital
City
Ankara
State/Province
Kec.oren
ZIP/Postal Code
06380
Country
Turkey
Facility Name
Keçiören Education and Training Hospital
City
Ankara
State/Province
Keçiören
ZIP/Postal Code
06380
Country
Turkey

12. IPD Sharing Statement

Citations:
PubMed Identifier
20920766
Citation
Razi CH, Harmanci K, Abaci A, Ozdemir O, Hizli S, Renda R, Keskin F. The immunostimulant OM-85 BV prevents wheezing attacks in preschool children. J Allergy Clin Immunol. 2010 Oct;126(4):763-9. doi: 10.1016/j.jaci.2010.07.038.
Results Reference
background

Learn more about this trial

Effect of OM-85 BV on Wheezing Related Morbidity in Children With Recurrent Wheezing

We'll reach out to this number within 24 hrs