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Aerosolized Hypertonic Xylitol Versus Hypertonic Saline in Cystic Fibrosis (CF) Subjects

Randomized Controlled Study of Aerosolized Hypertonic Xylitol Versus Hypertonic Saline in Hospitalized Patients With Exacerbation of Cystic Fibrosis

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00928135
Enrollment
63
Registered
2009-06-25
Start date
2013-01-22
Completion date
2018-04-09
Last updated
2021-06-25

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

Conditions

Cystic Fibrosis

Brief summary

Cystic fibrosis (CF) lung disease is characterized by chronic bacterial colonization and recurrent infection of the airways. Lowering the airway surface liquid (ASL) salt concentration has been shown to increase activity of salt sensitive antimicrobial peptides. Xylitol is a 5-carbon sugar that can lower the ASL salt concentration, thus enhancing innate immunity. In this study, the investigators propose to test the safety and tolerability of aerosolized xylitol used daily for 2 weeks in subjects with cystic fibrosis. In a pilot, 2-week study, 60 subjects with cystic fibrosis with an FEV1(Forced expiratory volume in 1 second ) \>30% predicted will be randomized to receive aerosolized 7% hypertonic saline (5 ml) or 15% xylitol, (5 ml) twice a day for 14 days. The primary outcomes will be safety as assessed by FEV1 change from baseline, adverse events and respiratory symptom score. Outcomes for trend in efficacy include density of colonization of sputum, time to next exacerbation, sputum cytokines and revised CF quality of life questionnaire.

Detailed description

Cystic fibrosis (CF) lung disease is characterized by chronic bacterial colonization and recurrent infection of the airways. Disruption of the cystic fibrosis transmembrane conductance regulator chloride channels in subjects with CF results in altered fluid and electrolyte transport across the airway epithelium thereby initiating infections. These infections eventually destroy the lungs and contribute to significant morbidity and mortality in patients with CF. It is well known that antibacterial activity of innate immune mediators such as lysozyme and beta defensins in human airway surface liquid (ASL) is salt-sensitive; an increase in salt concentration inhibits their activity. Conversely, their activity is increased by low ionic strength. Lowering the ASL salt concentration and increasing the ASL volume might therefore potentiate innate immunity and therefore decrease or prevent airway infections in subjects with CF. Xylitol, a five-carbon sugar with low transepithelial permeability, which is poorly metabolized by bacteria can lower the salt concentration of both cystic fibrosis (CF) and non-CF epithelia in vitro. Xylitol is an artificial sweetener that has been successfully used in chewing gums to prevent dental caries; it has been used as an oral sugar substitute without significant adverse effects. It has also been shown to decrease the incidence of acute otitis media by 20-40%; nasal application to normal human subjects was found to decrease colonization with coagulase negative staphylococcus. We found that aerosolized iso-osmolar xylitol was safe in mice, healthy volunteers and stable subjects with CF when administered over a single day. In a recent study, we observed that single doses of 10% followed by 15% xylitol was well tolerated by subjects with cystic fibrosis who were stable. In this pilot study we propose to test the hypothesis that aerosolized hypertonic xylitol given daily for 2 weeks, will be safe and well tolerated and potentially lower the density of colonization in subjects with CF compared to hypertonic saline. We chose hypertonic concentration of xylitol to be comparable in part to hypertonic saline which is being offered as a routine treatment in hospitalized patients with CF exacerbation.

Interventions

DRUGXylitol

15% xylitol solution for aerosol; Dosage: 5 ml twice a day (BID)

DRUGHypertonic saline

7% hypertonic saline solution for aerosol; Dosage: 5 ml twice a day (BID)

Sponsors

Joseph Zabner
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

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

Inclusion criteria

* Subjects with CF (medical record evidence of CFTR(Cystic fibrosis transmembrane conductance regulator) mutation or sweat chloride test or nasal voltage difference, and 1 or more clinical findings of CF), * Age 12 or greater * FEV1 \> 30% predicted(within the last 14 days and oxygen saturation \> 90% on FiO2(fraction of inspired oxygen) ≤ 50%, * Admitted for an exacerbation, * Use of effective contraception in women, * Able to provide written informed consent.

Exclusion criteria

* Pregnancy, * History of asthma based on methacholine challenge or bronchial hyperresponsiveness on PFTS(Pulmonary Function Test), * Hemoptysis more than 60 mL within the last 30 days, * Use of any investigational study drug within the last 30 days, * Initiation of hypertonic saline within the last 30 days, * A serum creatinine 2 mg/dl or more * Active malignancy in the last year * Antibiotics for CF exacerbation as an outpatient in the last 2 weeks * B cepacia colonization * Waiting list for lung transplant * Lack of FEV1 data from the last 14 days * Previous participation in this study

Design outcomes

Primary

MeasureTime frameDescription
Change in FEV1 Percentage Predicted From Baseline14 daysChange in lung function (forced expiratory volume in 1 second) between baseline and Day 14

Secondary

MeasureTime frameDescription
Density of Colonization of Pseudomonas Aeruginosa Per Gram of Sputum14 daysMean difference from baseline of Sputum density expressed as log colony forming units between baseline and Day 14
Exacerbations During 6 Months Follow-up6 monthsnumbers of subjects that experienced an exacerbation during the 6 months follow-up

Countries

United States

Participant flow

Recruitment details

1. subject screen failed due to intolerance to hypertonic saline 2. subjects failed xylitol trial inhalation

Participants by arm

ArmCount
Hypertonic Saline
7% hypertonic saline given twice daily for 14 days
29
Xylitol
Xylitol given twice daily for 14 days
30
Total59

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject10

Baseline characteristics

CharacteristicHypertonic SalineXylitolTotal
Age, Continuous30.4 years
STANDARD_DEVIATION 12.8
29.7 years
STANDARD_DEVIATION 12.3
30.1 years
STANDARD_DEVIATION 12.4
Forced Expiratory volume % predicted53.3 Percentage predicted
STANDARD_DEVIATION 18.8
58.8 Percentage predicted
STANDARD_DEVIATION 20.1
56.1 Percentage predicted
STANDARD_DEVIATION 19.5
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants0 Participants1 Participants
Race (NIH/OMB)
White
28 Participants30 Participants58 Participants
Sex: Female, Male
Female
12 Participants15 Participants27 Participants
Sex: Female, Male
Male
17 Participants15 Participants32 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 290 / 30
other
Total, other adverse events
11 / 298 / 30
serious
Total, serious adverse events
2 / 290 / 30

Outcome results

Primary

Change in FEV1 Percentage Predicted From Baseline

Change in lung function (forced expiratory volume in 1 second) between baseline and Day 14

Time frame: 14 days

ArmMeasureValue (MEAN)
7% Hypertonic SalineChange in FEV1 Percentage Predicted From Baseline11.8 percentage of predicted
Hypertonic XylitolChange in FEV1 Percentage Predicted From Baseline8.8 percentage of predicted
Secondary

Density of Colonization of Pseudomonas Aeruginosa Per Gram of Sputum

Mean difference from baseline of Sputum density expressed as log colony forming units between baseline and Day 14

Time frame: 14 days

Population: Subjects who were able to produce sputum at baseline and day 14

ArmMeasureValue (MEAN)
7% Hypertonic SalineDensity of Colonization of Pseudomonas Aeruginosa Per Gram of Sputum-1.4 log CFU/ml
Hypertonic XylitolDensity of Colonization of Pseudomonas Aeruginosa Per Gram of Sputum-0.9 log CFU/ml
Secondary

Exacerbations During 6 Months Follow-up

numbers of subjects that experienced an exacerbation during the 6 months follow-up

Time frame: 6 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
7% Hypertonic SalineExacerbations During 6 Months Follow-up15 Participants
Hypertonic XylitolExacerbations During 6 Months Follow-up11 Participants

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026