Early Intervention in Cystic Fibrosis Exacerbation
Completed · Not applicable
Conditions studied: Cystic Fibrosis
In brief
Individuals with cystic fibrosis (CF) develop chronic lung infections and suffer intermittent acute exacerbations of their lung disease. Most exacerbations are not treated until they cause increased symptoms, and patients seek medical attention. This proposal details a study of home lung function and symptom monitoring. Subjects will be randomly assigned to one of two groups: 1) home monitoring, in which spirometry and symptoms are recorded; or 2) standard care. The home monitoring data will be transmitted electronically to the study center. If spirometry or symptoms have deteriorated substantially, treatment for a CF pulmonary exacerbation will be initiated. It is anticipated that use of home monitoring will lead to earlier, more reliable recognition and treatment of exacerbations, which will translate into better lung health.
Key facts
- Study ID
- NCT01104402
- Run by
- Johns Hopkins University
- People needed
- 267
- Starts
- 2011-10-01
- Expected to finish
- 2015-09-01
- Last updated by the study team
- 2017-10-23
Who can join
Age: 14 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- CF diagnosis confirmed with sweat test, abnormal nasal potential difference and/or genetic testing
- Age 14 and older
- Able to perform spirometry
- Clinically stable without antibiotic treatment for a pulmonary exacerbation in the two weeks prior to the screening visit
- Forced expiratory volume in the first second (FEV1) greater than 25% of predicted at screening
You may not qualify if…
- History of solid organ transplant
- Participation in any interventional trial within the last 30 days
- Inability to speak and read the English language well enough to complete questionnaires
- Colonization with Burkholderia cepacia genomovar III within the last 24 months
- Currently receiving antimicrobial treatment specifically used to treat active non-tuberculosis mycobacterium
- Confirmed diagnosis of allergic bronchopulmonary aspergillosis (ABPA) as defined by the Cystic Fibrosis Foundation (CFF) guidance document that is being actively treated
Where it is running
- Johns Hopkins University CF Clinic — Baltimore, Maryland, United States
- University of Washington — Seattle, Washington, United States
- Seattle Children's Hospital — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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