NCT01508078

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.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial recruitment is currently suspended
Enrollment
259

participants targeted

Target at P75+ for all trials

Timeline
1mo left

Started May 2010

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
suspended

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

Study Progress99%
May 2010Jul 2026

Study Start

First participant enrolled

May 1, 2010

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

January 6, 2012

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 11, 2012

Completed
14.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Last Updated

September 5, 2025

Status Verified

September 1, 2025

Enrollment Period

16.2 years

First QC Date

January 6, 2012

Last Update Submit

September 3, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Airway inflammation

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

    Cross-sectional

Study Arms (2)

Asthmatics

Otherwise healthy asthmatic subjects

Healthy controls

Healthy individuals without evidence of pulmonary disease.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Asthmatics and healthy control

You may qualify if:

  • Age 18 years and older

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of California, San Francisco

San Francisco, California, 94143, United States

Location

Related Links

Biospecimen

Retention: SAMPLES WITH DNA

Samples of induced sputum and blood for DNA and RNA extraction, plasma, and serum will be banked in the UCSF Airway Tissue Bank.

MeSH Terms

Conditions

Asthma

Condition Hierarchy (Ancestors)

Bronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesRespiratory HypersensitivityHypersensitivity, ImmediateHypersensitivityImmune System Diseases

Study Officials

  • John Fahy, MD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 6, 2012

First Posted

January 11, 2012

Study Start

May 1, 2010

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

July 1, 2026

Last Updated

September 5, 2025

Record last verified: 2025-09

Locations