Official Title: “Efficacy of Amiloride and Hypertonic Saline in Cystic Fibrosis”

The purpose of this research study is to determine whether the combination of inhaled amiloride and a concentrated salt solution is better than the salt solution itself for cystic fibrosis (CF) patients. In CF, airway secretions are thick and dehydrated. Many patients use inhaled salt solutions to help draw water into their secretions so that they are easier to get rid of with chest physiotherapy (“chest PT”) and cough. Unfortunately, these salt solutions are reabsorbed very quickly by the airways, so the beneficial effects may not last very long. In the hopes of prolonging their effects, the drug amiloride could be used in combination to slow salt and water reabsorption from airways. Amiloride is a medication that has been given by mouth for high blood pressure for many years. It is possible that the combination of salt solutions and inhaled amiloride may significantly improve the clearance of secretions in CF, which would be expected to improve lung function in CF.

Study Type: Interventional

Study Design: Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study

Intervention(s) in this Clinical Trial

• Drug: 7% NaCl
• Drug: Amiloride HCl

Primary Measures

• FEV1

Secondary Measures

• Mucociliary clearance rate
• Quality of Life
• FVC
• FEF25-75
• Cough clearance rate

Inclusion Criteria:

• Established diagnosis of CF
• 2 gene mutations identified, or
• Sweat chloride > 60 mmol/L, and
• 1 or more typical CF clinical features
• Age > 14 years
• Able to perform spirometry and have post-bronchodilator FEV1 > 50% of predicted at screening
• Oxyhemoglobin saturation (by pulse oximetry) > 92% on room air
• Able to provide informed consent

Exclusion Criteria:

• Unstable lung disease:
• FEV1 > 15% below best clinical measurement within 6 months
• Requirement for IV antibiotics within 4 weeks of screening
• Requirement for any change in pulmonary medication within 2 weeks of screening
• Evidence of reactive airways
• Clinical diagnosis of asthma
• > 15% increase in FEV1 after bronchodilator at screening
• Hypertonic saline use within 2 weeks of screening
• Unwilling or unable to either continue or discontinue cyclical therapies (e.g. inhaled tobramycin) for the 2 weeks prior to screening and the entire study period
• Pregnancy, breast-feeding, or unwillingness to use barrier contraception during the entire study period
• History of allergy or intolerance to amiloride, hypertonic saline, quinine, albuterol, or related compounds
• Renal insufficiency (creatinine > 1.5 mg/dl)
• Hyperkalemia (K+ > 5.0 meq/L)
• Investigational drug use within 30 days of screening
• Radiation exposure within the past year that would exceed Federal Regulations by participating in the study

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 14 Years

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Sponsor: University of North Carolina

Overall Clinical Trial Officials and Contacts

Scott H. Donaldson, MD Principal Investigator University of North Carolina  

Information obtained from ClinicalTrials.gov on October 07, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00274391

Study ID Number: DONALDS00A0

ClinicalTrials.gov Identifier: NCT00274391

Health Authority: United States: Food and Drug Administration