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

Felix Ratjen

Status

Completed

Conditions

Observational

Treatments

Other: This is an observational study, no intervention used.

Study type

Observational

Funder types

Other

Identifiers

NCT03138772

1000055762

Details and patient eligibility

About

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.

Full description

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.

Enrollment

146 patients

Sex

All

Ages

3 to 16 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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