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

Study results available
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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

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01880723 on ClinicalTrials.gov