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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04703023
Other study ID # MUCUS2020
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 9, 2020
Est. completion date May 17, 2023

Study information

Verified date May 2023
Source Institut für Pneumologie Hagen Ambrock eV
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pilot basic research study on the properties of bronchial mucus. Examination of the sorption and desorption properties, mucin concentration, and structure of the mucus from healthy airways compared to patients with Chronic Obstructive Pulmonary Disease (COPD).


Description:

Mucus, of the correct composition, maintains airway hydration and protects the airway from inhaled particles through mucociliary transport. In chronic inflammatory airway diseases such as COPD or cystic fibrosis, infectious agents, inflammatory cells and products of inflammation such as DNA, increase mucus viscosity which results in decreased mucociliary clearance of inhaled particles, increasing the likelihood of respiratory infections. This pilot study is planned as basic research on the properties of bronchial mucus. Water isotherms and efficient water activity (sorption and desorption) of the collected samples are examined in defined temperature and humidity settings using DVS Intrinsic (Dynamic Vapour Sorption System, Surface Measurement Systems, London, UK). Findings will provide insights into possible treatment programs targeted at altering specific mucus components.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date May 17, 2023
Est. primary completion date May 2, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age>18 - COPD or other disease requiring bronchoscopy or elective surgery - Signed informed consent form Exclusion Criteria: - Not able to consent - Linguistic, cognitive, or other obstacles

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Kliniken Essen-Mitte, Evang. Huyssens-Stiftung/Knappschaft gGmbH Essen NRW

Sponsors (1)

Lead Sponsor Collaborator
Georg Nilius, Prof DR med

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sorption Maximum water sorption per degree of saturation in percent of the dry mass weight of the mucus samples 5 days
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