Measures of Respiratory Health Registry
Recruiting now
Conditions studied: Respiratory Disease, Cystic Fibrosis
In brief
There are many techniques that can allow for the quantification of lung function in children; some are being used clinically and others are under development. Many of these tools are available at BC Children's Hospital. This registry study will act as a central repository for the results of traditional and novel pulmonary function tests done at BC Children's Hospital to allow for future analysis.
Key facts
- Study ID
- NCT05501587
- Run by
- University of British Columbia
- People needed
- 1000
- Starts
- 2018-10-11
- Expected to finish
- 2028-05-01
- Last updated by the study team
- 2022-08-15
Who can join
Age: any, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of CF as evidenced by one or more clinical feature consistent with the CF phenotype or positive CF newborn screen AND one or more of the following criteria: i. A documented sweat chloride ≥ 60 mEq/L by quantitative pilocarpine iontophoresis (QPIT).
- ii. A documented genotype with two disease-causing mutations in the CFTR gene.
- In the opinion of the investigator, the participant will likely have the ability to perform the lung function test of interest on the day of testing
You may not qualify if…
- Physical findings at the screening that would compromise the safety of the participant or the quality of the data (e.g. respiratory distress or work of breathing)
- Requirement of supplementary oxygen to maintain oxygen saturation above 95%
- Participants with other Respiratory Disease
- Inclusion criteria:
- Physician-diagnosed lung disease
- Informed consent by participant, parent, or legal guardian
- In the opinion of the investigator, the participant will likely have the ability to perform the lung function test of interest on the day of testing
- Exclusion criteria
- Physical findings at screening that would compromise the safety of the participant or the quality of the research data
- Requirement of supplementary oxygen to maintain oxygen saturation above 95%
- Healthy Participants
- Inclusion criteria
- Informed consent by participant, parent, or legal guardian
- In the opinion of the investigator, the participant will likely have the ability to perform the lung function test of interest on the day of testing
- Exclusion criteria
- Physical findings at screening that would compromise the safety of the participant or the quality of the research data
- Evidence of lung disease
Where it is running
- British Columbia Children's Hospital — Vancouver, British Columbia, Canada (enrolling)
Full record on ClinicalTrials.gov
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