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Hypertonic Saline and Mucociliary Clearance in Children

Acute Inhalation of Hypertonic Saline Does Not Improve Mucociliary Clearance in All Children With Cystic Fibrosis

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01293084
Enrollment
17
Registered
2011-02-10
Start date
2007-07-31
Completion date
2009-06-30
Last updated
2015-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Keywords

mucociliary clearance, children, cystic fibrosis, hypertonic saline

Brief 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.

Detailed description

Several studies report that mucociliary clearance (MCC) is impaired in adults with CF. Because MCC is an important airway defense mechanism, drugs that slow impairment of MCC in children could prove beneficial in the long-term prognosis of the disease. A few studies have shown that inhalation of hypertonic saline (HS) significantly improves MCC in adults with CF and improvement is associated with increases in pulmonary function and decreases in pulmonary exacerbations. Nevertheless, no studies have examined if HS improves MCC in CF children. This is problematic for physicians who care for CF children with normal pulmonary function, since it is unclear if they should treat with HS or not. This study was designed to begin to answer this question. Twelve children with CF (7-12 yrs; 5 males) and normal pulmonary function (FEV1 and FVC \> 90% of predicted values) participated in a screening visit and two study visits. On the screening visit, children underwent an induced sputum test. On the two study visits, they inhaled 0.12% saline (placebo), or HS, in a double-blind, randomized, cross-over study. Following inhalation of placebo or HS, patients inhaled the radioisotope 99mtechnetium and underwent sequential imaging of their lungs with a gamma camera for 90 min and approximately 24 hrs later. Mucociliary clearance was quantified at 60 min (MCC60), 90 min (MCC90) and 24 hrs (MCC24hrs) after inhalation of the radioisotope. Between the 60 min and 90 min measurements, children coughed 30 times.

Interventions

DRUG0.12% saline

5mL of 0.12% saline inhaled once over 20 minutes

DRUG7% saline

5mL 7% saline inhaled once over 20 minutes

Sponsors

Cystic Fibrosis Foundation
CollaboratorOTHER
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
7 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Males and females * Age 7-12 years old * Diagnosis of cystic fibrosis by sweat chloride \> 60 meq/L, or presence of two CFTR mutations known to cause CF * Routinely treated with the short-acting bronchodilator albuterol * FEV1 \> 90% of predicted values

Exclusion criteria

* FEV1 \< 90% of predicted values * Routine use of hypertonic saline, mannitol, or amiloride * Allergic bronchopulmonary aspergillosis (ABPA) * Sputum colonization with Burkholderia cepacia or multiple antibiotic resistant organisms * Evidence of a pulmonary exacerbation within past two weeks * Treated with intravenous or oral antibiotics in the past two weeks for a pulmonary exacerbation * Presence of an acute respiratory illness characterized by: * Coughing above baseline values * Wheezing * Respiratory distress * Hemoptysis * Cannot perform the inhalation maneuvers that are required for drug inhalation or radioaerosol administration

Design outcomes

Primary

MeasureTime frame
Percent Mucociliary Clearance at 60 Minutes60 minutes

Secondary

MeasureTime frame
Percent Mucociliary Clearance at 90 Minutes90 minutes

Participant flow

Pre-assignment details

Data could not be retrieved for the order of randomization.

Participants by arm

ArmCount
Children With CF
Children with CF inhaled either 5 mL of 7% saline or 0.12% saline once over 20 minutes. On a second visit, the same children were crossed-over and inhaled either 0.12% saline or 7% saline over 20 minutes. The order of these visits was randomized but the sequence of the randomization is not known.
12
Total12

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyPhysician Decision3
Overall StudyWithdrawal by Subject2

Baseline characteristics

CharacteristicChildren With CF
Age, Continuous10.5 years
FEV1 (% predicted)108 percent predicted
FVC (% predicted)107 percent predicted
Genotype
F508del homozygous
9 participants
Genotype
F508heterozygous
2 participants
Genotype
Other
1 participants
Region of Enrollment
United States
12 participants
Sex: Female, Male
Female
7 Participants
Sex: Female, Male
Male
5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 120 / 12
serious
Total, serious adverse events
0 / 120 / 12

Outcome results

Primary

Percent Mucociliary Clearance at 60 Minutes

Time frame: 60 minutes

Population: Participants that completed received both 7% saline and 0.12% saline over the duration of the study

ArmMeasureValue (MEDIAN)
7% SalinePercent Mucociliary Clearance at 60 Minutes18.6 percentage mucociliary clearance
0.12% SalinePercent Mucociliary Clearance at 60 Minutes15.4 percentage mucociliary clearance
p-value: 0.62Wilcoxon (Mann-Whitney)
Secondary

Percent Mucociliary Clearance at 90 Minutes

Time frame: 90 minutes

Population: Data for participants that completed and received both 7% saline and 0.12% saline.

ArmMeasureValue (MEDIAN)
7% SalinePercent Mucociliary Clearance at 90 Minutes27.4 percentage mucociliary clearance
0.12% SalinePercent Mucociliary Clearance at 90 Minutes19.3 percentage mucociliary clearance
p-value: 0.32Wilcoxon (Mann-Whitney)

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026