MedPath

Saline Hypertonic in Preschoolers + CT

Phase 2
Completed
Conditions
Cystic Fibrosis
Interventions
Drug: Active Treatment Group 7% Hypertonic Saline
Drug: Control Group 0.9% Isotonic Saline
Registration Number
NCT02950883
Lead Sponsor
University of Washington, the Collaborative Health Studies Coordinating Center
Brief Summary

The purpose of this study is to assess whether inhalation of 7% hypertonic saline (HS) twice daily for 48 weeks reduces structural lung disease as assessed by computed tomography (CT) in comparison with inhalation of 0.9% isotonic saline (IS) in preschool children (ages 3 to 6) with cystic fibrosis.

Detailed Description

Several observational studies have shown that cystic fibrosis (CF) patients less than or equal to 6 years of age have clinically silent airway damage. There is growing interest in early initiation of therapies to prevent or delay the progression of this lung disease in CF. In SHIP-CT, the investigators will evaluate treatment effects of HS relative to IS on measures of structural lung disease obtained from chest CT using a novel scoring system sensitive to early lung changes, the Perth-Rotterdam Annotated Grid Morphometric Analysis method for CF (PRAGMA-CF), that quantifies the volume percentage of diseased airways (%Dis), bronchiectasis (%Bx), and trapped air (%TA). As a secondary evaluation of structural airway damage, the investigators will use an image analysis system to measure airway dimensions relative to adjacent arteries (AA-system). Longitudinal changes in CT measures will also be compared to changes in lung function measured by the lung clearance index (LCI) obtained by N2 Multiple Breath Washout (MBW) and to clinical outcomes.

The primary hypothesis is that HS will reduce structural lung disease as assessed by the PRAGMA-CF computed tomography score relative to IS during the 48-week treatment period among preschool children with CF.

SHIP-CT is a parallel study to SHIP001 (ClinicalTrials.gov Identifier NCT02378467). The primary hypothesis of SHIP001, which runs in North America, is that compared to IS, HS will improve the LCI, a measure of ventilation heterogeneity, during the 48-week treatment period among preschool children with CF. The SHIP-CT study (SHIP002) will use a nearly identical study design as the SHIP001 study, with similar eligibility criteria and treatment arms, to determine whether HS reduces structural lung disease as measured by chest computed tomography (CT), in addition to stabilizing or improving functional outcomes as measured by LCI.

This is a multicenter, randomized, double-blind, controlled, parallel group trial assessing structural lung disease in children with CF ages 3 to 5 at enrollment. Participants will be randomized 1:1 to receive 7% hypertonic saline (treatment arm) vs. 0.9% isotonic saline (control arm) administered twice daily via jet nebulizer for 48 weeks. Study visits will occur at screening, enrollment, and at Weeks 12, 24, 36, and 48. Parents or the legal guardian will be contacted at Weeks 1, 4 and 8 to document changes in health status, adverse events, concomitant medications/treatments, and encourage study treatment compliance. Parents or the legal guardian will also be contacted approximately every 6 weeks between visit 3, 4, 5, and 6 to address individual issues or concerns related to study treatment or study participation, and to document changes in health status, medications and treatments.

Total duration of participant participation will be up to 53 weeks. As enrollment will occur over approximately 18 months, total duration of the study is expected to be up to 30 months (18 months enrollment plus 12 months for the last participants to complete study participation).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
116
Inclusion Criteria
  1. Diagnosis of CF as evidenced by one or more clinical features consistent with the CF phenotype or positive CF newborn screen AND one or more of the following criteria:

    1. A documented sweat chloride ≥ 60 mEq/L by quantitative pilocarpine iontophoresis (QPIT)
    2. A documented genotype with two disease-causing mutations in the CFTR gene
  2. Informed consent by parent or legal guardian

  3. Age ≥ 36 months and ≤72 months at screening visit

  4. Ability to comply with medication use, study visits and study procedures as judged by the site investigator

  5. Ability to cooperate with chest CT at the enrollment visit as determined by the lung function technician

Exclusion Criteria
  1. Chest CT within 8 months prior to the Screening visit
  2. Acute intercurrent respiratory infection, defined as an increase in cough, wheezing, or respiratory rate with onset within 3 weeks preceding screening or enrollment visit
  3. Acute wheezing at screening or enrollment visit
  4. Oxygen saturation < 95% (<90% in centers located above 4000 feet elevation) at screening or enrollment visit
  5. Other major organ dysfunction, excluding pancreatic dysfunction
  6. Physical findings that would compromise the safety of the participant or the quality of the study data as determined by site investigator
  7. Investigational drug use within 30 days prior to screening or enrollment visit
  8. Treatment with inhaled HS at any concentration within 30 days prior to screening or enrollment visit
  9. Initiation (i.e. new prescription) of any inhaled hydrating agent such as mannitol or mucolytic agents such as dornase alpha within 30 days prior to the screening or enrollment visit
  10. Chronic lung disease not related to CF
  11. Inability to tolerate first dose of study treatment at the enrollment visit

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Active Treatment GroupActive Treatment Group 7% Hypertonic Saline7% Hypertonic Saline administered via inhalation twice daily for 48 weeks
Control GroupControl Group 0.9% Isotonic Saline0.9% Isotonic Saline administered via inhalation twice daily for 48 weeks
Primary Outcome Measures
NameTimeMethod
Chest CT48 weeks

The difference in PRAGMA-CF %Dis between HS and IS study arm at end of study (48 weeks), adjusted for baseline, measured from standardized chest CT.

Secondary Outcome Measures
NameTimeMethod
PRAGMA-CF Sub-scores48 weeks

i) The difference in PRAGMA-CF sub-scores, %Bx (the volume proportion of the lung with bronchiectasis) and %TA (the volume proportion of the lung with trapped air), between the baseline CT and the 48 week CT.

ii) The absolute number of airways, airway dimensions and AA ratios from TLC CTs, acquired at the 48-week visit.

Lung Clearance Index (LCI)48 weeks

The difference in LCI, measured by N2 MBW, from baseline to 48 weeks

Cross-sectional and longitudinal relationships48 weeks

Cross-sectional and longitudinal relationships between primary and secondary PRAGMA-CF outcomes (%Dis, %Bx and %TA) and MBW outcomes (LCI), airway dimensions and PRAGMA-CF and MBW outcomes, as well as CFQ-R scores and PRAGMA-CF and MBW

Trial Locations

Locations (25)

Washington University School of Medicine

🇺🇸

Saint Louis, Missouri, United States

John Hunter Children's Hospital

🇦🇺

Newcastle, Australia

Perth Children's Hospital

🇦🇺

West Perth, Australia

Children's Hospital of Colorado

🇺🇸

Aurora, Colorado, United States

Oregon Health Sciences University

🇺🇸

Portland, Oregon, United States

Hospital Robert Debre

🇫🇷

Paris, France

Riley Hospital for Children

🇺🇸

Indianapolis, Indiana, United States

Royal Women's and Children Hospital

🇦🇺

Adelaide, Australia

Sydney Children's Hospital at Randwick

🇦🇺

Sydney, Australia

British Columbia Children's Hospital

🇨🇦

Vancouver, British Columbia, Canada

Children's Hospital at Westmead

🇦🇺

Sydney, Australia

Hospice Civils de Lyon

🇫🇷

Lyon, France

Seattle Children's Hospital

🇺🇸

Seattle, Washington, United States

Copenhagen University Hospital Rigshospitalet

🇩🇰

Copenhagen, Denmark

Hospital Universitari Vall d'Hebron

🇪🇸

Barcelona, Spain

Children's Hospital of Pittsburgh of UPMC

🇺🇸

Pittsburgh, Pennsylvania, United States

University of North Carolina at Chapel Hill

🇺🇸

Chapel Hill, North Carolina, United States

Lady Cilento Children's Hospital

🇦🇺

Brisbane, Australia

Royal Children's Hospital

🇦🇺

Melbourne, Australia

Universitair Ziekenhuis Children's Hospital

🇧🇪

Brussels, Belgium

UZ Leuven - Gasthuisberg Ziekenhuis

🇧🇪

Leuven, Belgium

Hospital for Sick Kids

🇨🇦

Toronto, Ontario, Canada

Sophia Children's Hospital at Erasmus Medical Centre

🇳🇱

Rotterdam, Netherlands

Ospedale Civile Maggiore

🇮🇹

Verona, Italy

Bambini Gesu Children's Hospital

🇮🇹

Roma, Italy

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