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Completed

NCT Number: NCT03138772

Tracking CF Lung Disease Through the Early Years: Utility of the LCI

This is a prospective observational study to follow a cohort of patients with Cystic Fibrosis and healthy controls for a period of two years. This study will include monitoring the subjects lung clearance index (by performing a breathing test called the multiple breath washout), as well as spirometry and their respiratory symptoms every three months as well as during a pulmonary exacerbation and after their recovery.

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Key information

Conditions

Age range

3 year–16 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital for Sick Children

Toronto, Ontario, M5G1X8, Canada

About this study

This is a prospective observational cohort study. During the 3 year study period, each participant will be followed for a period of 2 years. The study will include quarterly measurements of the lung clearance index (LCI), as well as spirometry, for CF patients at their routine clinic visits. Parents of patients with CF will be asked to call the study nurse or clinical nurse if they experience a worsening of pulmonary symptoms and to come to the clinic for assessment of lung function. CF patients will then be assessed by a CF physician to assess whether they require antibiotic treatment based on a clinicians decisions to treat with antibiotics. The treatment decision will be left to the discretion of the patient's responsible physician, who will be blinded to the MBW results. All patients who meet the symptom based definition of a pulmonary exacerbation, regardless of treatment decision, will have MBW measured after 4 weeks. Following these visits at the time of an exacerbation, patients will have their MBW measured at their next clinic visit (usually within 3 months), and every 3 months thereafter until the end of the 2 year observation period, or the repeat onset of symptoms.This study will capture a maximum of two exacerbations per patient over the 2 year study period.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for Healthy Controls:

  • Informed consent by patient or parent/legal guardian, verbal assent where appropriate
  • Age 3 years to 16 years old
  • Clinically stable with no signs of an acute exacerbation at enrollment visit
  • Previously participated in a longitudinal MBW study at the Hospital for Sick Children and at the Riley Hospital for Children

Inclusion criteria

for CF Patients:

  • Diagnosis of CF as defined by two or more clinical features of CF and a documented sweat chloride > 60 mEq/L by quantitative pilocarpine iontophoresis test or a genotype showing two well characterized disease causing mutations
  • Informed consent by patient or parent/legal guardian, verbal assent where appropriate
  • Age 3 years to 16 years old
  • Clinically stable with no signs of an acute exacerbation at enrollment visit

Exclusion criteria

  • Previous organ transplantation
  • Chronic lung disease not related to CF, such as asthma
  • Use of intravenous antibiotics or other course of oral antibiotics (excluding maintenance treatment antibiotics) within 14 days of enrollment visit
  • Physical findings at screening that would compromise the safety of the participant or the quality of the study data

Treatment and study plan

This is an observational study, no intervention used.

Other

No intervention is being used in this study.

Primary outcomes

  1. Lung Clearance Index

    Time frame: an average of 2 years

    Outcome measure from the Multiple Breath Washout test.

Secondary outcomes

  1. Spirometry

    Time frame: an average of 2 years

    FEV1

  2. Respiratory Cultures

    Time frame: an average of 2 years

    Bacterial pathogens IL-8 and neutrophil elastase

  3. Respiratory Symptoms

    Time frame: an average of 2 years

    CFQ-R

  4. Respiratory Symptoms

    Time frame: an average of 2 years

    CFRSD-CRISS

Sponsors and collaborators

Lead sponsor

Felix Ratjen

Other

Registry information

Acronym: LCITRACK

Important dates

Study start
2017
Primary completion
2020
Study completion
2021
First posted
May 3, 2017
Registry last updated
Sep 21, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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