Measures of Respiratory Health Registry
NCT05501587 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2022-08-15
Summary
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.
Conditions
- Respiratory Disease
- Cystic Fibrosis
Sponsors & Collaborators
-
University of British Columbia
lead OTHER
Principal Investigators
-
Jonathan Rayment, MDCM, MSc · University of British Columbia
Eligibility
- Min Age
- 0 Years
- Max Age
- 99 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-10-11
- Primary Completion
- 2028-05-31
- Completion
- 2028-05-31
Countries
- Canada
Study Locations
More Related Trials
-
Evaluating Sensations of Breathlessness in Patients With Cystic Fibrosis
NCT01799642 ·Status: COMPLETED
-
Registry Study on Cystic Fibrosis in Chinese Children
NCT02753374 ·Status: NOT_YET_RECRUITING
-
Using MRI to Observe Lung Changes in Infants With CF Compared to Infants Without CF
NCT01832519 ·Status: COMPLETED
-
Inflammatory and Microbiologic Markers in Sputum: Comparing Cystic Fibrosis With Primary Ciliary Dyskinesia
NCT01155115 ·Status: COMPLETED ·Phase: NA
-
Evaluating the Impact of Chronic Rhinosinusitis on the Health-Related Quality of Life Among Adults With Cystic Fibrosis
NCT02003079 ·Status: COMPLETED
-
MR Imaging of Lung in the Follow-up Assessment of Cystic Fibrosis
NCT03357562 ·Status: COMPLETED ·Phase: NA
-
Hyperpolarized Xenon MRI in Cystic Fibrosis Pulmonary Exacerbations
NCT02606487 ·Status: COMPLETED
-
Home Monitoring to Predict Exacerbation in Cystic Fibrosis
NCT02416375 ·Status: COMPLETED
-
Changes in Lung Function Based on Differences in Spirometry Equipment Used in Children With Cystic Fibrosis
NCT01343524 ·Status: COMPLETED
-
Near Patient Microbial Testing in Cystic Fibrosis
NCT01877707 ·Status: COMPLETED ·Phase: NA
-
Assessment of Fat Free Mass Index and Its Impact on Health in Children With Cystic Fibrosis
NCT01401439 ·Status: COMPLETED
-
MRI in Cystic Fibrosis and Primary Ciliary Dyskinesia
NCT03279965 ·Status: UNKNOWN
-
19F MRI in Healthy Children and Children With Mild Cystic Fibrosis Lung Disease
NCT06066723 ·Status: RECRUITING
-
Molecular Diagnosis of Respiratory Viral Infections on Sputum From Cystic Fibrosis Patients
NCT03736096 ·Status: COMPLETED
-
Prediction of Survival in Children With Cystic Fibrosis Using the Multiple-breath Washout
NCT04016194 ·Status: COMPLETED
-
Respiratory Muscle Training in CF Patients
NCT03190031 ·Status: COMPLETED ·Phase: NA
-
Tracking CF Lung Disease Through the Early Years: Utility of the LCI
NCT03138772 ·Status: COMPLETED
-
Cardiopulmonary Fitness in Children With Cystic Fibrosis Compared to Healthy Children
NCT06242951 ·Status: COMPLETED
-
Viral Infections and Airway Microbiome in Young Children With Cystic Fibrosis
NCT06188988 ·Status: ENROLLING_BY_INVITATION
-
Assessment of CFTR-Modulator Treatment in Cystic Fibrosis Lung Disease Using Novel Structural and Functional MRI
NCT04391322 ·Status: ACTIVE_NOT_RECRUITING
-
Evaluation of Lung T1-MRI in Pediatric Cystic Fibrosis Patients
NCT04994301 ·Status: COMPLETED
-
19F MRI to Evaluate Regional Ventilation in Healthy Subjects and Subjects With Cystic Fibrosis
NCT03489590 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Controlled Ventilation CT in CF Infants
NCT01200888 ·Status: TERMINATED
-
Feasibility of Home-based Exercise Program for Adults With Cystic Fibrosis
NCT05239611 ·Status: COMPLETED ·Phase: PHASE2
-
Tissue Collection From People With Cystic Fibrosis
NCT00015756 ·Status: COMPLETED