NCT00603629

Brief Summary

The purpose of this study is to investigate mechanisms which cause acute asthma exacerbations by examining blood and airway secretions during an acute onset (sputum or tracheal aspirates). This pilot study is intended to uncover new mechanisms of asthma exacerbation and to generate hypotheses for future study. By collaborating with Genentech, we (scientists at UCSF) plan to incorporate the latest scientific findings into our work to discover and develop new treatments for asthma.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
23

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 2008

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2008

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

January 16, 2008

Completed
13 days until next milestone

First Posted

Study publicly available on registry

January 29, 2008

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2009

Completed
Last Updated

May 1, 2026

Status Verified

September 1, 2011

Enrollment Period

1.7 years

First QC Date

January 16, 2008

Last Update Submit

April 27, 2026

Conditions

Keywords

Acute Asthma

Outcome Measures

Primary Outcomes (1)

  • gene expression in blood and airway secretions and tissues

    Comparison of gene expression in blood and airway secretions and tissues during acute asthma exacerbation to recovery

    6 - 10 weeks

Study Arms (1)

I

People with acute asthma in the Emergency department or inpatient settings

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

People with acute asthma who seek treatment in the Emergency Department or who require admission to the hospital for their asthma

You may qualify if:

  • Male and female subjects aged 18 - 70 years
  • Medical history of asthma
  • Currently experiencing an acute exacerbation of asthma
  • Ability to provide informed consent or have a surrogate provide consent.
  • Ability to provide sputum.

You may not qualify if:

  • Cigarette smoking: Subjects must be non-smokers. Non-smokers are defined as subjects who have never smoked or who have not smoked for 1 year and have a total pack-year smoking history \< 10 packs.
  • Pregnant women.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UCSF Airway Clinical Research Center

San Francisco, California, 94143, United States

Location

Related Links

Biospecimen

Retention: SAMPLES WITH DNA

whole blood, DNA, RNA, sputum, nasopharyngeal swab

MeSH Terms

Conditions

Asthma

Condition Hierarchy (Ancestors)

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

Study Officials

  • John V Fahy, M.D., M.Sc.

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor in Residence

Study Record Dates

First Submitted

January 16, 2008

First Posted

January 29, 2008

Study Start

January 1, 2008

Primary Completion

September 1, 2009

Study Completion

September 1, 2009

Last Updated

May 1, 2026

Record last verified: 2011-09

Locations