Status:

COMPLETED

Biological Determinants of Sputum Rheology in Chronic Airway Diseases

Lead Sponsor:

University Hospital, Montpellier

Collaborating Sponsors:

APARD Fonds de dotation

Conditions:

Asthma

COPD

Eligibility:

All Genders

18+ years

Brief Summary

The primary objective of this study is to investigate the biological determinants of sputum rheology variations.

Detailed Description

Secondarily, this study aims to compare rheology parameters between different chronic airway disease sub-populations.

Eligibility Criteria

Inclusion

  • Affiliate with or beneficiary of the French national single-payer health insurance system
  • Patient capable of spontaneous mucus expectoration
  • Consulting or hospitalized at the study centre
  • Inclusion Criteria for the Asthma Group
  • Never- or former-smoker (\<10 pack-years)
  • Medical history compatible with asthma
  • Reversible post-brochodilator (or post-corticosteroid test) ventilatory obstruction (ratio of forced expiratory volume in 1 second : forced vital capacity \< 70%) or significant variation in respiratory function -- OR -- Bronchial hyperresponsiveness demonstrated during a broncho-provocation test
  • Inclusion Criteria for the COPD Group
  • Current- or former-smokers (\>10 pack years)
  • Chronic obstructive pulmonary disease according to GOLD criteria
  • Inclusion Criteria for the Bronchiectasis Group
  • Presence of bronchiectasis on computed tomography scan
  • Cystic fibrosis has been ruled out

Exclusion

  • Patient expresses opposition to the protocol
  • Breast feeding or pregnant
  • Metastatic neoplastic disease
  • Other active pulmonary disease (tuberculosis, interstitial lung disease)
  • Recent psychiatric disorder (in the past year and documented via a specialist consult)
  • Consumption of illicit drugs or alcoholism
  • Patients in an exclusion period determined by another study
  • Patients under any type of legal guardianship
  • Prisoners
  • Impossible to correctly inform the patient
  • Does not fluently read French
  • Emergency situations

Key Trial Info

Start Date :

September 15 2019

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

October 15 2019

Estimated Enrollment :

48 Patients enrolled

Trial Details

Trial ID

NCT04081740

Start Date

September 15 2019

End Date

October 15 2019

Last Update

November 7 2019

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Arnaud de Villeneuve Hospital

Montpellier, France, 34295