Hypertonic Saline and Mucociliary Clearance in Children
Status:
Completed
Trial end date:
2009-06-01
Target enrollment:
Participant gender:
Summary
Previously, the investigators and others have shown that mucociliary clearance (MCC) is
defective in patients with cystic fibrosis (CF) and it is now thought that alterations in
airway mucus rheology figure prominently in the impairment. Mucociliary clearance works by
trapping toxic particles, bacteria and viruses in the lung mucus and then quickly removing
the mucus out of the lungs. Defects in MCC typically lead to the accumulation of mucus in the
airways, and this in turn is associated with acute infections, chronic bacterial colonization
and chronic inflammation. One treatment strategy that is gaining acceptance as an important
therapy for improving MCC in adults with CF is the inhalation of the osmotic stimulus,
hypertonic saline (HS). A number of studies have shown that acute inhalation of HS (7%
saline) significantly improves MCC in adults with CF and results from a recent study indicate
that two weeks of inhaling HS leads to a significant increase in MCC that is sustained for 8
hours post inhalation and is associated with significant improvements in FEV1, FVC and
FEF25-75 values. Since MCC in patients with CF appears to be impaired by adulthood, any drug
that disrupts or slows the impairment in childhood could prove enormously beneficial in the
long-term prognosis of the disease. Nevertheless, no studies have been conducted to determine
if HS treatment improves MCC in children with CF. This is most problematic for physicians who
care for children with CF who have normal FEV1 and FVC values, since it is unclear if they
should treat these children with HS or not. This research study is designed to begin to
answer this question. The investigators hypothesize that acute inhalation of hypertonic
saline (7%) will improve MCC in CF children with normal pulmonary function. Our hypothesis
will be tested in a one-year clinical trial that will be randomized and placebo-controlled.
Twelve children with CF who are 7-12 years old and have normal FEV1 and FVC values will
participate. Our goal will be to compare MCC in these children on two study visits after
acute inhalations of placebo (0.12% saline) or hypertonic saline (HS) (7% saline) aerosol.
The investigators predict that MCC values after acute inhalation of 7% HS aerosol will be
statistically significantly greater than after placebo inhalation.
Phase:
Phase 2
Details
Lead Sponsor:
Johns Hopkins University
Collaborators:
Cystic Fibrosis Foundation Cystic Fibrosis Foundation Therapeutics