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Conditions
Interventions
Group 1: The PROVID-CAPSyS study will include adult hospitalized patients with SARS-CoV-2 infection / COVID-19 with severe course and ventilation. The PROVID-CAPSyS target of N=60 evaluable patients i
Sponsors
Charité – Universitätsmedizin Berlin, Med. Klinik m. S. Infektiologie und Pneumologie und Arbeitsbereich pulmonale Inflammation
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Positive detection of SARS-CoV-2-virus, ventilation (invasive, non-invasive, high-flow, ECMO), informed consent
Exclusion criteria
Exclusion criteria: Patient participation in PROVID-CAPNETZ, PROVID-PROGRESS or PROVID-CAPSyS at an earlier time, simultaneous participation in PROVID-CAPNETZ, pregnancy, breast feeding, active tuberculosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| death | — |
Secondary
| Measure | Time frame |
|---|---|
| Length of hospitalization length of ICU treatment length of mechanical ventilation organ involvement (complications) long-term effects changes in quality of life | — |
Countries
Germany
Contacts
Public ContactAgata Mikolajewska
Charité - Universitätsmedizin BerlinMedizinische Klinik mit Schwerpunkt Infektiologie und Pneumologie
Outcome results
None listed