NCT00201266

Brief Summary

This study will evaluate the link between blood group antigens and asthma exacerbations.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
126

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2005

Longer than P75 for all trials

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

July 1, 2005

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

September 16, 2005

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 20, 2005

Completed
5.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2011

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2013

Completed
Last Updated

March 9, 2026

Status Verified

March 1, 2026

Enrollment Period

6.1 years

First QC Date

September 16, 2005

Last Update Submit

March 5, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Asthma exacerbations requiring prednisone

    Prior 2 years

Secondary Outcomes (1)

  • Lung fuction

    Current

Study Arms (2)

Exacerbation resistant asthma

Control group

Procedure: Screening

Exacerbation prone asthma

Cases

Procedure: Screening

Interventions

ScreeningPROCEDURE

Characterization tests including blood group typing, measures of lung function, measures of allergy, and collection of DNA.

Exacerbation prone asthmaExacerbation resistant asthma

Eligibility Criteria

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

Asthmatics of two types: 1. Exacerbation resistant asthma (no requirement for prednisone for asthma since age 12). 2. Exacerbation prone asthma (requirement for prednisone for asthma in the past 2 years).

You may qualify if:

  • Diagnosis of asthma, as confirmed by methacholine responsiveness less than 8 mg/mL
  • History of asthma exacerbation in the 2 years prior to study entry requiring treatment with oral corticosteroids

You may not qualify if:

  • Cigarette smoking in the 10 years prior to study entry or total pack per year history greater than 10
  • History of asthma exacerbations requiring treatment with oral corticosteroids since age 12 (control group)

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 Publications (1)

  • Innes AL, McGrath KW, Dougherty RH, McCulloch CE, Woodruff PG, Seibold MA, Okamoto KS, Ingmundson KJ, Solon MC, Carrington SD, Fahy JV. The H antigen at epithelial surfaces is associated with susceptibility to asthma exacerbation. Am J Respir Crit Care Med. 2011 Jan 15;183(2):189-94. doi: 10.1164/rccm.201003-0488OC. Epub 2010 Aug 23.

Biospecimen

Retention: SAMPLES WITH DNA

DNA, plasma, saliva, induced sputum.

MeSH Terms

Conditions

AsthmaLung Diseases

Interventions

Mass Screening

Condition Hierarchy (Ancestors)

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

Intervention Hierarchy (Ancestors)

Diagnostic Techniques and ProceduresDiagnosisHealth SurveysSurveys and QuestionnairesData CollectionEpidemiologic MethodsInvestigative TechniquesDiagnostic ServicesPreventive Health ServicesHealth ServicesHealth Care Facilities Workforce and ServicesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public HealthPublic Health Practice

Study Officials

  • John V. Fahy

    University of California, San Francisco

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 16, 2005

First Posted

September 20, 2005

Study Start

July 1, 2005

Primary Completion

August 1, 2011

Study Completion

August 1, 2013

Last Updated

March 9, 2026

Record last verified: 2026-03

Locations