Skip to main content
Clinical Trials/NCT01759186
NCT01759186Active, not recruitingNot Applicable

Severe Asthma Research Program

The Cleveland Clinic5 sites in 1 country300 target enrollmentStarted: December 1, 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
300
Locations
5
Primary Endpoint
Identify metabolic mechanism(s) and age dependent change in the epidemiology of asthma

Study Overview

Brief Summary

The investigators will study the biologic and chemical differences that cause the greater incidence, and severity of asthma in women as compared to men. Severe asthma affects boys more than girls, while severe asthma in adults is predominantly a disease of women. The investigators aim to identify the processes that occur in the body that are behind the onset of severe asthma in young women during the teenage years, and the resolution of severe asthma in boys. To further evaluate gender influences on asthma, asthmatic women at different stages of their menstrual cycle (period) will be also studied. The investigators aim to use biomarkers to develop testing procedures that will identify different types or characteristics of asthma in men and women; and to follow patients over time to uncover relevant clinical outcomes of biomarkers. The investigators anticipate that they will 1) develop clinically relevant tests to identify unique types or characteristics of asthma and severe asthma; 2) determine outcomes over time of biochemically-defined types of asthma; and 3) identify the reasons for why adult women are affected more than men with severe asthma.

Detailed Description

This scientific site-specific project is part of a larger network of asthma studies, the Severe Asthma Research Program (SARP). The mission of SARP is to improve the understanding of severe asthma to develop better treatments.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
6 Years to 80 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Subjects with asthma
  • children age 6-17 years old (25% enrollment)
  • adults 18 years and older (75% enrollment)

Exclusion Criteria

  • Pregnancy during the characterization phase
  • Current smoking
  • Smoking history > 10 pack years if ≥30 years of age, or smoking history > 5 pack years if <30 years of age (Note: if a subject has a smoking history, no smoking within the past year),
  • Other chronic pulmonary disorders associated with asthma-like symptoms, including (but not limited to) cystic fibrosis, chronic obstructive pulmonary disease, chronic bronchitis, vocal cord dysfunction (that is the sole cause of respiratory symptoms and at the PI's discretion)
  • Severe scoliosis or chest wall deformities
  • History of premature birth before 35 weeks gestation
  • Unwillingness to receive an intramuscular triamcinolone acetonide injection.

Outcomes

Primary Outcomes

Identify metabolic mechanism(s) and age dependent change in the epidemiology of asthma

Time Frame: 5 years

To determine if asthma severity is worsened in females with changes in estradiol that occur during puberty as measured by asthma control tests and lung functions

Secondary Outcomes

  • Development of clinical testing procedures to assign metabolic asthma phenotypes(5 years)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Serpil Erzurum

multiple Prinicipal Investigators [B Gaston, S. Erzurum, G. Teague]

The Cleveland Clinic

Study Sites (5)

Loading locations...

Similar Trials