Patienthèque of Finisterian (South of Brittany) Children With Cystic Fibrosis in the Time of Precision Medicine
NCT04137133 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2024-04-23
Summary
The objective of this study is to evaluate the relevance of Porphyromonas as a biomarker predicting the risk of P. aeruginosa primocolonization in children form 0 to 18 years old with cystic fibrosis.
Conditions
Interventions
- DIAGNOSTIC_TEST
-
collection
bronchial secretions, blood, stools, superficial skin sample, dental plaque sample and urine
Sponsors & Collaborators
-
University Hospital, Brest
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-03-21
- Primary Completion
- 2030-03-31
- Completion
- 2030-03-31
Countries
- France
Study Locations
More Related Trials
-
Tracking CF Lung Disease Through the Early Years: Utility of the LCI
NCT03138772 ·Status: COMPLETED
-
Epidemiology of Anaerobic Bacteria in Cystic Fibrosis Patients: Descriptive and Non-interventional Study
NCT04879381 ·Status: COMPLETED
-
Evaluation of the Evolution of Quality of Life in Relation to Naso-sinus Symptomatology Under Treatment With CFTE Modulators in Children Aged 6 to 11 Years With Cystic Fibrosis With Compatible Mutation
NCT05581056 ·Status: COMPLETED
-
Evaluation of the Lung Clearance Index
NCT02342951 ·Status: COMPLETED ·Phase: NA
-
Cellular Markers in Treated or Untreated Non-tuberculous Mycobacterial Respiratory Infection in Patients With Cystic Fibrosis
NCT06602869 ·Status: RECRUITING
-
Biodistribution of Neutrophile Proteases in the Sputum of Patients Affected by Cystic Fibrosis
NCT00750932 ·Status: COMPLETED
-
Cystic Fibrosis Diagnosis by Analyzing Nasal Brushing
NCT02433132 ·Status: UNKNOWN ·Phase: NA
-
Description of the Short-term Effects of KAFTRIO® by Continuous Monitoring With the PHEAL-CR-K Application in Real Life in Patients With Cystic Fibrosis Eligible for KAFTRIO® Treatment
NCT05295524 ·Status: UNKNOWN ·Phase: NA
-
Response to CFTR Modulators in CF Patients Under 18 Years
NCT04301856 ·Status: RECRUITING
-
Characterization of Pulmonary Microbiome in Cystic Fibrosis Patients
NCT04735679 ·Status: UNKNOWN
-
A Safety and Tolerability Study OF PUR118 In Subjects With Cystic Fibrosis
NCT01543191 ·Status: COMPLETED ·Phase: PHASE1
-
The Use of Breath Volatile Organic Compounds in Early Detection of Acute Pulmonary Exacerbations in Cystic Fibrosis
NCT05944367 ·Status: COMPLETED
-
Analysis T Cells Response for Identification of Aspergillus Bronchitis With Cystic Fibrosis Patients
NCT02550041 ·Status: TERMINATED ·Phase: NA
-
Sputum Validation for the Molecular Diagnosis of Respiratory Viral Infections in Cystic Fibrosis
NCT03684759 ·Status: COMPLETED
-
Validation of Therapeutic Efficacy Targeting the Splicing Variants in Cystic Fibrosis and CFTR Pathologies
NCT05100823 ·Status: TERMINATED ·Phase: NA
-
Home Monitoring to Predict Exacerbation in Cystic Fibrosis
NCT02416375 ·Status: COMPLETED
-
Near Patient Microbial Testing in Cystic Fibrosis
NCT01877707 ·Status: COMPLETED ·Phase: NA
-
The EPIC Observational Study
NCT00676169 ·Status: COMPLETED
-
Prospective Study of the Phenotypic Expression of Cystic Fibrosis (CF) Screened Positive Newborns With an Atypical Form of CF (DPAM)
NCT02869932 ·Status: COMPLETED ·Phase: NA
-
Pharmacokinetic Study of Aerosolized Colimycin in Cystic Fibrosis
NCT01537614 ·Status: COMPLETED ·Phase: PHASE1
-
Registry to Monitor the Susceptibility to Aztreonam of Pseudomonas Aeruginosa Isolates From Cystic Fibrosis Patients
NCT01375036 ·Status: COMPLETED
-
Early Intervention in Pulmonary Exacerbation in Cystic Fibrosis
NCT00850551 ·Status: COMPLETED ·Phase: NA
-
Non-Invasive Biomarkers in Cystic Fibrosis
NCT00413140 ·Status: COMPLETED
-
Small Circulating RNA as Molecular Markers of Lung Disease in Cystic Fibrosis
NCT02992080 ·Status: COMPLETED ·Phase: NA
-
Functional Analysis by Dynamic Imaging of the Respiratory Epithelium in Infants With Cystic Fibrosis
NCT01605565 ·Status: COMPLETED ·Phase: NA