Clinical Trial Details
— Status: Recruiting
Administrative data
| NCT number |
NCT02496468 |
| Other study ID # |
DZL_DA_AA-1 |
| Secondary ID |
|
| Status |
Recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
January 2013 |
| Est. completion date |
December 2023 |
Study information
| Verified date |
December 2020 |
| Source |
Klinikum der Universitaet Muenchen |
| Contact |
Esther Zeitlmann, Diplom |
| Phone |
+49894400 |
| Email |
esther.zeitlmann[@]med.uni-muenchen.de |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
Despite its common occurrence, still little is known about pathomechanisms determining
different wheeze and asthma trajectories and phenotypes in children, and those beginning in
adulthood. Therefore, deciphering underlying determinants for different childhood and adult
asthma phenotypes is urgently needed to develop personalized treatment approaches targeting
distinct underlying mechanisms. Thereby, secondary prevention early in the disease process
can also be achieved. The decoding of such mechanisms and their translation to the individual
patient is the aim of the Disease Area Asthma Allergy of the 'German Centre for Lung
Research' (DZL).
Description:
About 25-30% of children have at least one episode of wheeze before their 3rd birthday, but
considerable clinical heterogeneity exists. Many of these children become symptom-free
between 3 and 8 years of age, but some go on to persistent asthma in later childhood and
adulthood. Despite its high prevalence, still little is known about pathomechanisms
determining the different wheeze trajectories and phenotypes in children, and those beginning
in adulthood. Frequency and severity of exacerbations may play an important role in the
chronification process but underlying mechanisms are equally not well understood. Therefore,
deciphering the role of airway mechanics, genetic, environmental and molecular determinants
for different childhood and adult asthma phenotypes for exacerbations and chronification
processes is urgently needed to develop personalized treatment approaches targeting distinct
underlying mechanisms. Thereby, secondary prevention early in the disease process can also be
achieved.
In order to do so, a clinical cohort for childhood asthma has been set up with identical,
standardized instruments (quality assurance plan: standard operating procedures (SOPs) for
clinical and lab modules, shipment, biobanking and analysis as well as quality control
measures via audits and site visits have been developed) across the participating 'German
Center for Lung Research' (DZL) sites. Here, new-onset steroid/leukotriene receptor
antagonist (LTRA) naïve wheeze/asthma patients and wheeze/asthma patients under controller
therapy are being recruited in addition to healthy controls. Following recruitment, regularly
follow-ups and exacerbation visits of included patients are being performed with identical
study instruments and meticulous quality control checks as at baseline.
PROJECT HYPOTHESES:
1. Specific molecular phenotypes are associated with distinct wheeze/asthma phenotypes and
trajectories. Thereby, underlying mechanisms as well as predictors and biomarkers for
persistent asthma will be identified.
2. Individuals at risk for exacerbations can be identified by clinical and molecular
biomarkers, which will become novel targets for therapy and secondary prevention.
WORK PROGRAM:
Identification of molecular phenotypes, predictors and biomarkers for distinct wheeze/asthma
phenotypes and trajectories.
The investigators aim to recruit over 1000 cases and controls to ensure sufficient
statistical power for multivariate statistical analyses. Recruitment of study participants
will be continued and cases will undergo 'deep phenotyping' as described below. In addition,
healthy age and sex matched controls will be recruited. Cases and controls undergo a
comprehensive clinical assessment including questionnaires (browser-based online data entry
into extensive database with audit trail, plausibility and quality control checks
implemented, data dictionary accessible), physical examination and lung function tests
(spirometry and bodyplethysmography including bronchodilator response, multiple breath
washout, exhaled nitric oxide). Biomaterials will be collected for analyses: i) blood
samples; ii) nasal secretions; iii) pharyngeal swabs; iv) induced sputum; v) stool samples.
Furthermore, epithelial cells will be collected by nasal brushings. Breath samples will be
collected for analyses of volatile organic compounds. The cases will be followed up regularly
using the same clinical tools and collecting the same biomaterials as at the initial visit to
assess trajectories over time. Two closely interacting working groups have been established
for all aims described: one lab and one data management/analysis group, each headed by expert
members of the participating sites. The lab group will initiate and supervise all
measurements of biomaterials; the data management/analysis group will expand the combined and
shared data base and coordinate statistical analyses across sites. A common publication
policy has already been developed. Using advanced bioinformatics, systems biology and machine
learning approaches, the investigators will develop predictive (diagnostic) algorithms
including clinical and molecular biomarkers for transient and persistent wheeze/asthma
phenotypes and their trajectories. These analyses will also identify underlying mechanisms
and thereby potential targets for future personalized therapy comparing childhood and adult
findings. During data collection. The investigators attempt to minimize missing data. In all
cases where missing data will reduce power for subsequent analyses, imputation will be used
in order to omit power loss.
