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Mechanisms of Exacerbation of Asthma

Mechanisms of Exacerbation of Asthma

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00594750
Acronym
MECA
Enrollment
67
Registered
2008-01-16
Start date
2006-05-01
Completion date
2025-08-05
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Brief summary

The purpose of this study is to identify the causes of asthma that were not previously suspected, to better understand the effects of inhaled steroids on asthma and to identify new way to treat asthma.

Detailed description

In this study, we will explore mechanisms of exacerbation in asthma by careful characterization studies in asthmatics presenting in acute severe exacerbation. Specifically, we will determine the frequency of secretor status in these subjects by blood and saliva testing, and we will also perform a detailed cellular and biochemical analysis of their airway secretions. We will collect airway secretions using two methods. One method will be to have subjects cough sputum into a clean plastic container. The other method only applies to asthmatics with near-fatal asthma requiring intubation and mechanical ventilation. In these asthmatics, we will collect airway secretions by tracheal aspirate using methods normally applied in their clinical care.

Interventions

None listed

Sponsors

University of California, San Francisco
Lead SponsorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Male and female subjects with a history of asthma between the ages of 18 to 75 years. 2. Physician diagnosis of asthma. 3. Currently experiencing an acute exacerbation of asthma. This exacerbation may be severe necessitating treatment in the emergency room, ICU, or hospital ward. 4. Ability to provide informed consent.

Exclusion criteria

1. Lung disease other than asthma. 2. Females who are lactating or who are pregnant. 3. Use of recreational drugs in the 1 month preceding the study.

Design outcomes

Primary

MeasureTime frame
rheological measurements (viscosity and elasticity) in sputum from patients with acute severe asthma1-2 years

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJohn V Fahy, M.D., M.Sc.

University of California, San Francisco

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026