Small Circulating RNA as Molecular Markers of Lung Disease in Cystic Fibrosis
NCT02992080 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80
Last updated 2022-01-03
Summary
The aim of our study is to assess miRNAs expression profiles in the circuling blood of patients with cystic fibrosis and highlight "signatures" that could reflect the pulmonary status of patients
Conditions
Interventions
- OTHER
-
miRNAs isolation from blood samples of patients and control
Blood sample collection in specific PAXGene tubes
Sponsors & Collaborators
-
University Hospital, Montpellier
lead OTHER
Principal Investigators
-
Caroline RAYNAL, PharmD, PhD · Montpellier University Hospital (CHU Montpellier) Montpellier University
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 12 Months
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2016-07-12
- Primary Completion
- 2020-06-30
- Completion
- 2020-06-30
Countries
- France
Study Locations
More Related Trials
-
Evaluation of Sit-to-stand Test in Patients With Cystic Fibrosis and Matched Controls.
NCT03524859 ·Status: COMPLETED
-
The Relationship Between CFTR Gene Mutations and Exercise Capacity
NCT05157646 ·Status: WITHDRAWN ·Phase: NA
-
Microbial Community Composition and Dynamics in Lungs of Cystic Fibrosis Sibling Pairs
NCT00590330 ·Status: COMPLETED
-
Diagnosis and Treatment of Patients With Cystic Fibrosis
NCT00001223 ·Status: TERMINATED
-
Breath Analysis in in Adults With Cystic Fibrosis (CF)
NCT02209571 ·Status: COMPLETED ·Phase: NA
-
Assessment of CFTR-Modulator Treatment in Cystic Fibrosis Lung Disease Using Novel Structural and Functional MRI
NCT04391322 ·Status: ACTIVE_NOT_RECRUITING
-
Costimulatory Molecules as Biomarkers in Cystic Fibrosis
NCT01353950 ·Status: COMPLETED
-
Non-Invasive Biomarkers in Cystic Fibrosis
NCT00413140 ·Status: COMPLETED
-
Correction of Nonsense Mutations in Cystic Fibrosis
NCT03670472 ·Status: RECRUITING
-
The Role of Respiratory Viruses in Exacerbations of Cystic Fibrosis in Adults
NCT01238081 ·Status: COMPLETED
-
Molecular Diagnosis of Respiratory Viral Infections on Sputum From Cystic Fibrosis Patients
NCT03736096 ·Status: COMPLETED
-
Surrogate Markers of Response to New Therapies in Cystic Fibrosis Patients
NCT02965326 ·Status: RECRUITING ·Phase: NA
-
Validation of Therapeutic Efficacy Targeting the Splicing Variants in Cystic Fibrosis and CFTR Pathologies
NCT05100823 ·Status: TERMINATED ·Phase: NA
-
Combating Diagnostic Wandering and Impasse for Cystic Fibrosis
NCT05654480 ·Status: UNKNOWN
-
Prognostic Value of Functional Exercise Test (EFX) in Cystic Fibrosis
NCT02994017 ·Status: COMPLETED ·Phase: NA
-
Characterization of Pulmonary Microbiome in Cystic Fibrosis Patients
NCT04735679 ·Status: UNKNOWN
-
COVID-19 Antibody Responses In Cystic Fibrosis
NCT05158829 ·Status: UNKNOWN
-
Asthma With Hypersecretion-associated Gene for Cystic Fibrosis
NCT02558127 ·Status: COMPLETED
-
A Novel Assay to Quantify Treatment Response in Cystic Fibrosis (CF)
NCT01626157 ·Status: COMPLETED
-
Gene Modifiers of Cystic Fibrosis Lung Disease
NCT00037765 ·Status: ACTIVE_NOT_RECRUITING
-
Identification of New Biological Markers for the Progression of Mycobacterium Abscessus-induced Lung Disease in Cystic Fibrosis
NCT06413459 ·Status: RECRUITING
-
Molecular Phenotypes for Cystic Fibrosis Lung Disease
NCT01116414 ·Status: COMPLETED
-
Muscle Fatigue in People With Cystic Fibrosis: Insight From a Mobile App
NCT07135869 ·Status: COMPLETED
-
Muscle Accrual and Function in Cystic Fibrosis-Impact of Glucose Intolerance
NCT02776098 ·Status: COMPLETED
-
Biodistribution of Neutrophile Proteases in the Sputum of Patients Affected by Cystic Fibrosis
NCT00750932 ·Status: COMPLETED