CASA: Characterization of Adult Subjects for Asthmatic Research Studies

Sponsor
University of California, San Francisco (Other)
Overall Status
Recruiting
CT.gov ID
NCT01508078
Collaborator
(none)
2,000
1
146
13.7

Study Details

Study Description

Brief Summary

This study is designed to characterize subjects in terms of the nature and severity of their asthma and in terms of conditions that may alter the clinical expression of asthma. Some features will be obtained in all subjects. These include a medical history and baseline lung function tests. This characterization forms the basis for our database that facilitates research protocols.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The purpose of this study is to generate a cohort of well-characterized asthmatic subjects as a resource for recruitment of asthmatic subjects and healthy controls in clinical studies and clinical trials in the UCSF Airway Clinical Research Center. The UCSF Airway Clinical Research Center (ACRC) conducts multiple clinical research studies in asthma funded by the NIH, foundations, and industry. We have a broad range of research interests, but we have specific interests in mechanism-oriented clinical studies and specific expertise in biospecimen collection, biobanking, and biospecimen analysis. Our model is to have multiple studies recruiting simultaneously, and this means that we need well-organized recruitment and database systems.

    Additionally, we aim to characterize asthmatic subjects in multiple domains, including disease severity, airway inflammation subtypes, and mucus subtypes. Asthma is a heterogeneous disease in its clinical presentation and in its underlying cellular and molecular phenotypes. To explore cellular and molecular phenotypes of asthma, we will analyze induced sputum for cell types and gene expression, with a focus on Th2 inflammation pathways and innate and adaptive immune cells that drive Th2 inflammation. Detailed cellular analysis of sputum is possible but requires that multiple sputum samples be collected for processing in multiple different ways, including by cytocentrifugation, FACS analysis, and by formalin fixation and paraffin embedding of sputum cell pellets. We are also studying mucus phenotypes of asthma using methods of rheology, which needs to be done on fresh sputum.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    2000 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Characterization of Adult Subjects for Asthmatic Research Studies
    Study Start Date :
    May 1, 2010
    Anticipated Primary Completion Date :
    Jul 1, 2022
    Anticipated Study Completion Date :
    Jul 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Asthmatics

    Otherwise healthy asthmatic subjects

    Healthy controls

    Healthy individuals without evidence of pulmonary disease.

    Outcome Measures

    Primary Outcome Measures

    1. Airway inflammation [Cross-sectional]

      We will measure various indicators of airway inflammation and compare them with various phenotypic characteristics.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Age 18 years and older
    Exclusion Criteria:
    • History of lung disease other than asthma

    • An upper respiratory tract infection or an exacerbation of their asthma within the preceding 4-6 weeks.

    • Persons who have smoked > 5 cigarettes per month and have a total pack-year smoking history > 10 packs.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of California, San Francisco San Francisco California United States 94143

    Sponsors and Collaborators

    • University of California, San Francisco

    Investigators

    • Principal Investigator: John Fahy, MD, University of California, San Francisco

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    University of California, San Francisco
    ClinicalTrials.gov Identifier:
    NCT01508078
    Other Study ID Numbers:
    • 10-01627
    First Posted:
    Jan 11, 2012
    Last Update Posted:
    Feb 1, 2022
    Last Verified:
    Jan 1, 2022
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 1, 2022