Covid-19 Respiratory Sequelae French Cohort

NCT05075785 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2933

Last updated 2024-07-03

No results posted yet for this study

Summary

As the investigators need data on long term outcome of Covid-19, especially respiratory sequelae, a national cohort is required. To better evaluate the potential respiratory sequelae after SARS-CoV-2 infection, it is fundamental to include patients with different management at the acute phase of the Covid-19: ambulatory management, hospitalization in non ICU and in ICU units. That is why the investigators will conduct a national cohort study with all components of french pneumology which will give the investigators the opportunity to include patients in general hospital, in university hospital and in private structure. As it is a "real life" study, the investigators will include all patients who will have a consultation with a pneumologist for an evaluation 5 to 7 months after a Covid-19 infection whatever their acute disease management. The investigators will collect all available data on Covid-19 acute phase, on patients characteristics and comorbidities, on persistent symptoms after Covid-19, on exams results during the outcome evaluation (CT-scan, 6 min walk test, spirometry and DLCO, blood gas, VO2 max if realized).

Conditions

Sponsors & Collaborators

  • Cabinet Medical valenciennes

    collaborator UNKNOWN
  • CH Aix

    collaborator UNKNOWN
  • hopital privé de bois bernard

    collaborator UNKNOWN
  • Clinique La Croix du Sud

    collaborator UNKNOWN
  • University Hospital, Bordeaux

    collaborator OTHER
  • Hopital Forcilles

    collaborator OTHER
  • Hopital d'instructions des armées

    collaborator UNKNOWN
  • Hôpital Européen Marseille

    collaborator OTHER
  • Rennes University Hospital

    collaborator OTHER
  • Clinique Saint Augustin

    collaborator UNKNOWN
  • Delafontaine Hospital

    collaborator OTHER
  • Centre Hospitalier Universitaire de Saint Etienne

    collaborator OTHER
  • Centre Hospitalier de Troyes

    collaborator OTHER
  • Centre Hospitalier le Mans

    collaborator OTHER
  • University Hospital, Clermont-Ferrand

    collaborator OTHER
  • University Hospital, Tours

    collaborator OTHER
  • Centre Hospitalier Universitaire, Amiens

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-07
Primary Completion
2023-04-01
Completion
2024-05-01

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05075785 on ClinicalTrials.gov