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Exercise-Induced Bronchospasm in Cystic Fibrosis
This study is currently recruiting participants.
Study NCT00806455   Information provided by Ohio State University
First Received: December 9, 2008   No Changes Posted

December 9, 2008
December 9, 2008
July 2008
July 2012   (final data collection date for primary outcome measure)
To determine the prevalence of exercise-induced bronchospasm in a cohort of adolescent and adult patients with cystic fibrosis [ Time Frame: end of study ] [ Designated as safety issue: No ]
Same as current
No Changes Posted
  • To determine the prevalence of exercise-induced bronchospasm in those CF patients with evidence of allergic inflammation versus those without allergic inflammation. [ Time Frame: end of study ] [ Designated as safety issue: No ]
  • To determine the difference in exhaled nitric oxide and other surrogate markers of inflammation, as well as self-reported quality-of-life and symptom scores in CF patients with and without exercise-induced bronchospasm. [ Time Frame: end of study ] [ Designated as safety issue: No ]
Same as current
 
Exercise-Induced Bronchospasm in Cystic Fibrosis
Exercise-Induced Bronchospasm in Cystic Fibrosis

Exercise is an important clinical feature in cystic fibrosis. Better exercise capacity has been associated with better patient outcomes and quality of life. Exercise-induced bronchospasm is a condition, often associated with asthma, which may make exercise difficult. The role that exercise-induced bronchospasm has in people with cystic fibrosis is unknown. This study is designed to determine how often exercise-induced bronchospam occurs in cystic fibrosis.

We anticipate that Visit 1 will take approximately three hours. This will include obtaining informed consent, completing baseline demographic and quality of life questionnaires, brief physical exam, measuring exhaled nitric oxide level, skin allergy testing, obtaining blood and sputum samples, and performing pulmonary function testing before and after bronchodilators.

Visit 2 will take approximately two and one-half hours. This will include performing Eucapnic Voluntary Hyperventilation, measuring exhaled nitric oxide levels, and obtaining blood and sputum samples.

Visit 3 will take approximately two and one-half hours. This will include performing Cardiopulmonary exercise testing followed by serial spirometry, measuring exhaled nitric oxide levels, and obtaining blood and sputum samples.

 
Observational
Case-Only, Prospective
  • Cystic Fibrosis
  • Bronchospasm
 
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
40
July 2012
July 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Males and females with confirmed diagnosis of Cystic Fibrosis:

    • 2 positive sweat chloride tests (or)
    • genetic testing
  2. Age 12 years and older
  3. Baseline FEV1 ≥70% predicted
  4. Clinically stable over past 28 days:

    • no change in chronic respiratory symptoms
    • no need for antibiotics other then chronic maintenance therapies
    • no need for oral steroids
    • no increased use of bronchodilators
  5. Visit 1 FEV1 within 10% of baseline

Exclusion Criteria:

  1. History of Allergic Bronchopulmonary Aspergillosis (ABPA)
  2. Chronic airway colonization with Burkholderia cepacia (defined as 2 or more prior positive sputum or BAL cultures)
  3. Pregnancy
  4. Chronic oral corticosteroid use
  5. Febrile illness within two weeks of Visit 1
  6. Unable to provide consent (patients under age of 18 will require both parental consent AND patient assent)
  7. Current cigarette smoking, cessation of smoking within 6 weeks of Visit 1, or more than 10 pack-years of prior smoking
Both
12 Years and older
No
Contact: Janice E. Drake, CRRT 614-247-7707 john.mastronarde@osumc.edu
Contact: Sharon Cheung, BS 614-366-2258 sharon.cheung@osumc.edu
United States
 
NCT00806455
John G. Mastronarde, M.D. Associate Professor, The Ohio State University
2007H0319
Ohio State University
 
Principal Investigator: John G. Mastronarde, MD Ohio State University
Ohio State University
December 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP