Ireland
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Recruiting Observational

Retrospective and Prospective Cohort of Patients Entering the Multidisciplinary Management of Post-Covid Syndromes

NCT05805566 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2023-04-27
Last updated
2024-02-28

Condition(s) studied

Post-Covid Syndrome

Investigational drug(s) / intervention(s)

Blood collection

Blood collection: Blood samples will be collected from the patient at baseline. This blood will be collected during the standard of care blood drawing in extra.

Study summary

SARS-CoV2 pneumonia has been a global public health emergency since 2020. The prevalence of the disease is particularly high with more than 500 million cases worldwide (7.5 million in France) since the emergence of the virus.

A substantial proportion of patients with SARS-Cov2 infection present persistent symptoms long after the acute infection. This is independent of the degree of severity of the SARS-Cov2 infection.

These symptoms can affect the quality of life and impede the return to work. While the majority of symptoms progress favourably with outpatient care, some persist and/or are particularly severe, justifying expert and multidisciplinary care.

This investigation aim to create a clinical database of patients with complex and/or severe post-CoviD and study blood markers what could predict the disease and orientate new ways of treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: All patients who have joined the Epsilon care pathway since its opening in February 2022, i.e.: * Patients with post-Covid syndrome referred to the Epsilon sector from the city medicine: * Patient with documented SARS-Cov2 pneumonia * With persistent and severe symptoms beyond 4 weeks or complex or disabling symptoms beyond 3 months * Patient over 18 years old. Post-hospital sector: * Patient with documented SARS-Cov2 pneumonia * Hospitalized for oxygen therapy (at least 48h) * Not having a referring pulmonologist * Not institutionalized * With a life expectancy of more than 6 months. Exclusion Criteria: * Patient refusing that this data to be used for research purposes (objection form). * Patient with untreated comorbidities

Primary outcome measure(s)

  • Create a patient cohort — Once a year
    Creation of a retrospective and prospective cohort combining: * Collection of clinical and paraclinical data, scores, and scales. * Prospective monitoring of quality of life, other scores as needed. Cross-referencing of clinical data with the results of cellular and molecular analyzes on lymphocytes blood cells, which will be carried out (part carried out by Inserm). by INSERM U1111 as part of the European HERVCOV project.

Trial sites (1)

FacilityCityRegionStatus
Department of Acute Pneumology and Thoracic Oncology, Hôpital Lyon Sud, Hospices Civils de Lyon Pierre-Bénite France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05805566 on ClinicalTrials.gov ↗ ← All trials in France