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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01947218
Other study ID # 2013-A00553-42
Secondary ID 2013-14
Status Completed
Phase N/A
First received
Last updated
Start date June 30, 2014
Est. completion date August 7, 2023

Study information

Verified date August 2023
Source Assistance Publique Hopitaux De Marseille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Asthma and COPD are characterized by an accelerated decline in lung function associated with incompletely reversible airflow obstruction. This could be the result of lung structural changes and inflammation. Tissue repairing mechanisms may result in a restitution ad integrum of bronchial epithelium. But in most cases, especially in COPD and severe asthma, the "remodeling" is characterized by mucus cells hyperplasia, overproduction of mucus, and physicochemical, biological and immunological changes. Clinically, this mucus overproduction is reported by patients as the clinical symptom called "chronic bronchitis". Generally, it develops at a bronchiolar level where it is responsible for the progression of these diseases. There is a paradox, because the intrinsic properties of mucus seem rather beneficial so fighting against it may not be really wise at long-term. Especially its defensive effect against microbial agents which remains poorly explained. Currently, no treatment aims to reduce the production of mucus and mechanisms leading to such an overproduction are poorly understood in severe asthma and COPD. The identification of new targets to treat this overproduction of mucus in COPD is therefore of major interest. In view of current knowledge, inflammatory mediators and signal transduction leading to increased mucin production and increased number of goblet cells are probably IL-9, IL-13, IL -1ß and TNF-α involving calcium-sensitive chloride channels. Intracellular signaling pathways seem to be based on STAT-6, FOXA2, SPDEF, EGFR and / or COX-2


Recruitment information / eligibility

Status Completed
Enrollment 55
Est. completion date August 7, 2023
Est. primary completion date December 19, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - The patient must be given free and informed consent and signed the consent - The patient must be a member or beneficiary of a health insurance plan - Women and men are included (s) - The patient is aged at least 18 years Exclusion Criteria: - neoplastic disease extent - Other progressive lung disease (tuberculosis, diseases of the pulmonary interstitium, active or recent pulmonary infection.) - Patient unstable or had experienced exacerbation in the previous month study. - Unable to understand the nature and purpose of the study - Not affiliated to the French social security - Making their military or military service career - During periods of exclusion on another protocol - Patients who are mentally or legally can not give consent. - Patients with recent psychiatric disorders (less than a year). - The illicit drugs or alcohol. - Pregnant women, nursing mothers and women in labor; - Women of childbearing potential without effective contraception (specified in the protocol) - Persons deprived of their liberty by a judicial or administrative decision, hospitalized without consent and persons admitted to a health or social establishment for purposes other than research; - Minors; - The adults subject to a measure of legal protection or unable to consent; - The people in emergency situations can not give consent. - People with a cons-indication for bronchial biopsies (coagulation disorders, anticoagulation can be suspended ...)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
bronchial biopsies

Other:
Determination of CO in exhaled air


Locations

Country Name City State
France Assistance Publique Hopitaux de Marseille Marseille

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary measure the impact of cigarette smoke on the formation and composition of mucus produced by the bronchial epithelium (physicochemical properties, protein composition and potentially beneficial role in innate immunity) 4 years
Secondary measure the concentration of intracellular calcium induced by cigarette smoke measured by confocal microscopy using a fluorochrome (Fura-2) 4 years
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