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Inhaled Xylitol Versus Saline in Stable Subjects With Cystic Fibrosis

Randomized Cross Over Study of Inhaled Hypertonic Xylitol Versus Hypertonic Saline in Stable Subjects With Cystic Fibrosis

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01355796
Enrollment
30
Registered
2011-05-18
Start date
2011-05-31
Completion date
2015-02-28
Last updated
2018-10-24

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 plan to study the safety and efficacy of 2 weeks of inhaled xylitol compared to 2 weeks of hypertonic saline in a randomized crossover design in stable subjects with cystic fibrosis

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. The investigators 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, the investigators observed that single doses of 10% followed by 15% xylitol was well tolerated by subjects with cystic fibrosis who were stable. In this study, the investigators plan to study the safety and efficacy of 2 weeks of inhaled xylitol compared to 2 weeks of hypertonic saline in a randomized crossover design in stable subjects with cystic fibrosis

Interventions

DRUGXylitol

Aerosolized 15% xylitol, 5 ml twice a day for 2 weeks

DRUGHypertonic saline

4 ml of 7 % saline aerosolized twice a day for 2 weeks

Sponsors

Ann & Robert H Lurie Children's Hospital of Chicago
CollaboratorOTHER
Northwestern University
CollaboratorOTHER
Joseph Zabner
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Documented diagnosis of CF (medical record evidence of 2 identified CFTR(Cystic fibrosis transmembrane conductance regulator) mutations or a positive sweat chloride test or nasal voltage difference, and 1 or more clinical findings of CF) * Age 16 or greater * FEV1\>30% predicted * Oxygen saturation \> or equal too 90% on room air * Clinically stable, without evidence of pulmona4ry exacerbation for at least 2 weeks prior to screening (defined as use of oral or intravenous antibiotics for cystic fibrosis exacerbation) * Use of effective contraception in women * Ability to provide written informed consent and assent * Successful completion of the trial doses of study drugs

Exclusion criteria

* Pregnancy * Hemoptysis more than 100 mL within the last 30 days * Change in chronic medication within the last 30 days * History of elevated serum creatinine (\> than or equal to 2 mg/dl) within 30 days or at screening * History of lung and other solid organ transplantation * Wait-listed for lung or other solid organ transplant * Known intolerance to inhaled hypertonic saline

Design outcomes

Primary

MeasureTime frameDescription
Change in FEV1 % Predicted From BaselineBaseline and 14 daysChange from baseline in FEV1(maximal amount of air you can forcefully exhale in one second) % predicted

Secondary

MeasureTime frameDescription
Sputum Densitybaseline and 14 daysDifference from baseline in density of Pseudomonas aeruginosa colonization per gram of sputum,

Countries

United States

Participant flow

Participants by arm

ArmCount
All Participants
Baseline characteristics of the entire study cohort
30
Total30

Baseline characteristics

CharacteristicAll Participants
Age, Categorical
<=18 years
4 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
26 Participants
Age, Continuous31 years
STANDARD_DEVIATION 12.56
FEV171 % of predicted
Region of Enrollment
United States
30 participants
Sex: Female, Male
Female
15 Participants
Sex: Female, Male
Male
15 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 300 / 30
other
Total, other adverse events
1 / 301 / 30
serious
Total, serious adverse events
0 / 301 / 30

Outcome results

Primary

Change in FEV1 % Predicted From Baseline

Change from baseline in FEV1(maximal amount of air you can forcefully exhale in one second) % predicted

Time frame: Baseline and 14 days

ArmMeasureValue (MEAN)
XylitolChange in FEV1 % Predicted From Baseline-0.1 percentage of predicted
SalineChange in FEV1 % Predicted From Baseline1.4 percentage of predicted
p-value: <0.0595% CI: [-1.76, 4.75]Mixed Models Analysis
Secondary

Sputum Density

Difference from baseline in density of Pseudomonas aeruginosa colonization per gram of sputum,

Time frame: baseline and 14 days

Population: 27 out of 30 subjects were able to give sputum on day 14 and only those subjects are included in this analysis

ArmMeasureValue (MEAN)
XylitolSputum Density-1.98 Log colony forming units
SalineSputum Density0.93 Log colony forming units

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