LAIV (Flumist®) Administration in CF Patients
NCT01885169 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 170
Last updated 2014-09-16
Summary
Influenza (the "flu") is one of the most common respiratory viruses associated with respiratory deteriorations in children and adolescents with cystic fibrosis. These deteriorations usually mean antibiotics, hospitalizations, and worsening of pulmonary function tests. A new flu vaccine has been recently approved for use in Canada (Flumist®). What is particular about this flu vaccine is that it is a spray in the nose, which mimics how influenza usually infects us. This particular vaccine protects children and adolescents much better than the regular injectable flu shot.
This new vaccine has been given to \> 2,000 healthy children and to \>2,000 children with asthma and well tolerated. The investigators want to know if Flumist® is well tolerated in children with CF and does not cause worsening of respiratory symptoms. The investigators will conduct a study where all participants will receive Flumist® in the nose. This study is particularly important because its results will provide safety information on a vaccine that is more efficacious for a population who needs safe and easy to administer protection against the flu.
Conditions
Interventions
- BIOLOGICAL
-
Flumist®
The three cohorts will receive Flumist® and will be swabbed for inflammatory markers and viral shedding.
Sponsors & Collaborators
-
Ministere de la Sante et des Services Sociaux
collaborator OTHER -
Canadian Cystic Fibrosis Foundation
collaborator OTHER -
PHAC/CIHR Influenza Research Network
collaborator OTHER_GOV -
McGill University Health Centre/Research Institute of the McGill University Health Centre
lead OTHER
Principal Investigators
-
Caroline Quach-Thanh, MD, MSc · McGill University Health Centre/Research Institute of the McGill University Health Centre
-
Caroline Quach-Thanh, MD, MSc · McGill University Health Centre/Research Institute of the McGill University Health Centre
Eligibility
- Min Age
- 2 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2013-08-31
- Primary Completion
- 2014-04-30
- Completion
- 2015-12-31
Countries
- Canada
Study Locations
More Related Trials
-
Impact of Respiratory Viral Infections in Infants With Cystic Fibrosis.
NCT02847156 ·Status: COMPLETED ·Phase: NA
-
An Ocular Safety Study of Ivacaftor-Treated Pediatric Patients 11 Years of Age or Younger With Cystic Fibrosis
NCT01863238 ·Status: COMPLETED
-
Tissue Collection From People With Cystic Fibrosis
NCT00015756 ·Status: COMPLETED
-
Ivacaftor Treatment in 4 Month to 2 Year Old CF Subjects
NCT03783286 ·Status: COMPLETED
-
Real-life Follow-up of Cystic Fibrosis Patients Treated With Ivacaftor+Lumacaftor (Orkambi*)
NCT03475381 ·Status: COMPLETED
-
The Role of Respiratory Viruses in Exacerbations of Cystic Fibrosis in Adults
NCT01238081 ·Status: COMPLETED
-
Interferon Gamma-1b by Inhalation for the Treatment of Patients With Cystic Fibrosis
NCT00043316 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Viral Infections and Airway Microbiome in Young Children With Cystic Fibrosis
NCT06188988 ·Status: ENROLLING_BY_INVITATION
-
Microbiome Acquisition and Progression of Inflammation and Airway Disease in Infants and Children With Cystic Fibrosis
NCT01661491 ·Status: COMPLETED
-
Lum-Iva-biota: Exploring the Respiratory Mycobiota and Microbiota Profile in French CF Patients Taking Lumacaftor-Ivacaftor
NCT03565692 ·Status: UNKNOWN
-
Study of Ivacaftor in Cystic Fibrosis Subjects 2 Through 5 Years of Age With a CFTR Gating Mutation
NCT01705145 ·Status: COMPLETED ·Phase: PHASE3
-
Study of Interferon Gamma-1b by Injection for the Treatment of Patients With Cystic Fibrosis
NCT00043342 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Effect of Acid Blockade on Microbiota and Inflammation in Cystic Fibrosis (CF)
NCT02769637 ·Status: TERMINATED
-
Viral Pathogenesis of Early Cystic Fibrosis Lung Disease
NCT01973192 ·Status: COMPLETED
-
Microbial Community Composition and Dynamics in Lungs of Cystic Fibrosis Sibling Pairs
NCT00590330 ·Status: COMPLETED
-
Roll-Over Study of Ivacaftor in Cystic Fibrosis Pediatric Subjects With a CF Transmembrane Conductance Regulator Gene (CFTR) Gating Mutation
NCT01946412 ·Status: COMPLETED ·Phase: PHASE3
-
Microbial Community Composition and Metabolism in Cystic Fibrosis
NCT00954018 ·Status: COMPLETED
-
Study of INS37217 Inhalation Solution in Mild to Moderate Cystic Fibrosis Lung Disease
NCT00056147 ·Status: COMPLETED ·Phase: PHASE2
-
Pilot Study Testing the Effect of Ivacaftor on Lung Function in Subjects With Cystic Fibrosis and Residual CFTR Function
NCT01685801 ·Status: COMPLETED ·Phase: PHASE2
-
Ivacaftor in French Patients With Cystic Fibrosis and a G551D Mutation
NCT02194881 ·Status: COMPLETED
-
A Study of the Effects of Lumacaftor/Ivacaftor (LUM/IVA) on Exercise Tolerance in Subjects With Cystic Fibrosis (CF), Homozygous for the F508del-CFTR Mutation
NCT02875366 ·Status: COMPLETED ·Phase: PHASE4
-
Study of Ivacaftor in Subjects With Cystic Fibrosis (CF) Who Have a Non-G551D CF Transmembrane Conductance Regulator (CFTR) Gating Mutation
NCT01614470 ·Status: COMPLETED ·Phase: PHASE3
-
Alpha1 Antitrypsin Aerosol Therapy in Cystic Fibrosis
NCT02010411 ·Status: TERMINATED ·Phase: PHASE2
-
A Prospective, Multicenter, Collaborative Study to Determine the Prevalence of Nontuberculous Mycobacteria (NTM) in Pediatric Patients With Cystic Fibrosis in Florida
NCT02198079 ·Status: COMPLETED
-
A Study in Adult and Pediatric Patients With Cystic Fibrosis
NCT00034515 ·Status: COMPLETED ·Phase: PHASE1/PHASE2