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NCT05501587Recruiting

Measures of Respiratory Health Registry

Source: ClinicalTrials.gov · Last updated 15 Aug 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1000 (estimated)
First submitted
11 Aug 2022
Start date
11 Oct 2018
Primary completion date
31 May 2028
Lead sponsor
University of British Columbia
NCT number
NCT05501587

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 11 Oct 2018 to the primary completion date, 31 May 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Requirement of supplementary oxygen to maintain oxygen saturation above 95%
    • Participants with other Respiratory Disease
  • Evidence of lung disease

Other

  • 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)
  • 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
  • Physical findings at screening that would compromise the safety of the participant or the quality of the research data

Who the study is looking for

  • -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).
  • 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
  • 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

Criteria the registry did not label

  • Participants with CF

Age in the registry: 0 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
British Columbia Children's Hospital
Coordinator of this site? Confirm its status
VancouverCanadaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.