Development and Validation of a Sputum Biomarker mRNA Panel for the Diagnostic Work-up of Asthma 4.
BioSput-Air
1 other identifier
interventional
20
1 country
1
Brief Summary
The main objectives of the study are: 1\. To unravel the importance of molecular phenotyping in predicting the response to antimicrobial therapy with potential anti-inflammatory potency The investigators have developed a non-invasive technique based on mRNA analysis of induced sputum that enables us to study airway inflammation in detail. This technique forms the basis for our current project based on the following hypotheses:
- 1.Different molecular asthma phenotypes exist: a Th2 phenotype and a non Th2 phenotype as reported by Woodruff and colleagues (Woodruff PG et al). Sputum mRNA cytokine levels can be used to diagnose Th2 asthma and discriminate this from non-Th2 asthma.
- 2.Based on our previous research and preliminary data that non-Th2 asthma can be further divided in Th17 asthma and Th1+Th2 asthma; besides these, a fourth group without Th2, Th17 or Th1 characteristics also exist.
- 3.These subgroups have different responses to anti-microbial therapy with potential anti-inflammatory potency (macrolides).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2011
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 18, 2010
CompletedFirst Posted
Study publicly available on registry
October 20, 2010
CompletedStudy Start
First participant enrolled
July 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2019
CompletedJuly 13, 2018
July 1, 2018
7.4 years
October 18, 2010
July 12, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
sputum cytokine mRNA
3 months
Secondary Outcomes (1)
responsiveness to the medication
3 months
Study Arms (1)
azithromycin
OTHERInterventions
Eligibility Criteria
You may qualify if:
- severe asthmatics (GINA step 4 or step 5 (without anti-IgE))
You may not qualify if:
- viral/fungal/bacterial infection +fever (\<1 month)
- asthma exacerbation (\<3 months)
- other respiratory disease (CF, ciliary dyskinesia,bronchiectasis)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital of Leuven
Leuven, Vlaams-Brabant, 3000, Belgium
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Dominique MA Bullens, MD,PhD
Lab of clinical immunology, O&N I Herestraat 49 - bus 811, 3000 Leuven, België
- STUDY DIRECTOR
Sven F Seys, MSc
Lab of clinical immunology, O&N I Herestraat 49 - bus 811, 3000 Leuven, België
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- prof. dr.
Study Record Dates
First Submitted
October 18, 2010
First Posted
October 20, 2010
Study Start
July 1, 2011
Primary Completion
December 1, 2018
Study Completion
December 1, 2019
Last Updated
July 13, 2018
Record last verified: 2018-07