Utilizing Exhaled Breathe Condensate Collection to Study Ion Regulation in Cystic Fibrosis
NCT01880723 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32
Last updated 2023-11-29
Summary
Our aims were to determine if exhaled breath condensate (EBC) could detect differences in ion regulation between cystic fibrosis (CF) and healthy and measure the effect of the albuterol on EBC ions in these populations. We hypothesized EBC chloride and sodium would be lower in CF patients at baseline and that albuterol would decrease EBC sodium and increase EBC chloride.
Conditions
- Cystic Fibrosis
- Healthy
Interventions
- DRUG
-
Albuterol
2.5 mg diluted in 3mL normal saline nebulized using a Power Neb2 nebulizer
- DRUG
-
Placebo saline
nebulized 3mL normal saline) using a Power Neb2 nebulizer
Sponsors & Collaborators
-
National Heart, Lung, and Blood Institute (NHLBI)
collaborator NIH -
University of Arizona
lead OTHER
Principal Investigators
-
Wayne J Morgan, MD · Department of Pediatrics- Pulmonology, Allergy and Immunology, University of Arizona, Tucson, Arizona
-
Cori M Daines, MD · Department of Pediatrics- Pulmonology, Allergy and Immunology, University of Arizona, Tucson, Arizona
-
Eric M Snyder, PhD · Department of Pharmacy Practice and Science, University of Arizona, Tucson, Arizona
-
Hanna Phan, PharmD · Department of Pharmacy Practice and Science, University of Arizona, Tucson, Arizona
-
Asad Patanwalla, PharmD · Department of Pharmacy Practice and Science, University of Arizona, Tucson, Arizona
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 15 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-05-31
- Primary Completion
- 2012-07-31
- Completion
- 2013-01-31
Countries
- United States
Study Locations
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