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Clinical Trials/NCT04528901
NCT04528901UnknownNot Applicable

Study of seroPREvalence Vis-à-vis SARS-CoV2 and Correlation With Clinical Forms of COVID-19 in Patients Followed in Pneumology in the Cluster Area of the Grand-Est Region (Strasbourg University Hospital)

University Hospital, Strasbourg, France1 site in 1 country1,080 target enrollmentStarted: September 4, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
1,080
Locations
1
Primary Endpoint
Determine and compare the seroprevalence for SARS-CoV2 among patients with respiratory pathologies monitored in Pneumology at the Strasbourg University Hospital, in the cluster zone of the Grand Est.

Study Overview

Brief Summary

seroPREvalence vis-à-vis SARS-CoV2 and correlation with clinical forms of COVID-19 in patients followed in Pulmonology in the cluster area of the Grand-Est region.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Man or woman from 18 years old and without upper age limit
  • Patient followed in pulmonology at Strasbourg University Hospital
  • Patient presenting at least one of the following pathologies:
  • severe persistent asthma (200 patients)
  • chest cancer that is active or has received treatment within a period of less than one year (300 patients)
  • history of lung transplantation performed before the start of the epidemic (02/29/2020) (300 patients)
  • idiopathic or other diffuse interstitial lung disease, sarcoidosis or vasculitis (70 patients)
  • pulmonary arterial hypertension (PAH) (group 1 of the international classification) any cause or chronic thromboembolic PAH (group 4): (60 patients)
  • Severe COPD in the respiratory failure stage (150 patients)
  • Subject affiliated to a social health insurance protection scheme
  • Subject able to understand the objectives of the research
  • Subject having signed an informed consent

Exclusion Criteria

  • Inability to provide informed information about the subject (subject in an emergency situation, difficulty in understanding the subject, etc.)
  • Subject under safeguard of justice
  • Subject under guardianship or guardianship

Outcomes

Primary Outcomes

Determine and compare the seroprevalence for SARS-CoV2 among patients with respiratory pathologies monitored in Pneumology at the Strasbourg University Hospital, in the cluster zone of the Grand Est.

Time Frame: 15 months

Carrying out a serological assay of specific antibodies to SARS-CoV-2

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Strasbourg, France
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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