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RECRUITINGOBSERVATIONAL

COVIDOM: Longterm Morbidity of SARS-CoV-2 Infection and COVID-19 Disease - Consequences for Health Status and Quality of Life

COVIDOM: Longterm Morbidity of SARS-CoV-2 Infection and COVID-19 Disease - Consequences for Health Status and Quality of Life (NAPKON-POP)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

COVID-19 is a novel disease caused by SARS-CoV-2 that primarily affects the lungs but also various other organs of the body already in early stages of the disease. Due to the multiple organ involvements in the acute phase, it is conceivable that - in a significant proportion of patients - longterm sequels in various organ systems might occur, thereby impacting the individual's health status and quality of life; and posing a relevant burden to the resources of the health care system Assessment of SARS-CoV-2-longterm morbidity and sequels on the population level: In order to identify and treat these sequels in a timely fashion and to get a sense of the prevalence of such SARS-CoV-2 sequels on the population level, it is important to collect follow-up data and to comprehensively re-examine a population-representative sample of SARS-CoV-2 infected individuals. Within the COVIDOM study we will conduct deep clinical and biochemical phenotyping in population-representative samples in Germany. This will allow novel insights into disease pathogenesis and chronicity of virus infections.

Who May Be Eligible (Plain English)

Who May Qualify: - PCR-confirmed SARS-CoV-2 infection - living in one of the target areas - age at least 18 years - written willing to sign a consent form Who Should NOT Join This Trial: - Acute SARS-CoV-2 infection or reinfection Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * PCR-confirmed SARS-CoV-2 infection * living in one of the target areas * age at least 18 years * written informed consent Exclusion Criteria: * Acute SARS-CoV-2 infection or reinfection

Treatments Being Tested

OTHER

Observation of different courses of SARS-CoV-2 infection in different phases (acute vs. post-acute) and settings

Oberservatory Cohorts focusing (I) on subjects after SARS-CoV-2 infection that are recruited from the general population (POP), and on subjects with acute SARS-CoV-2 infections recruited (II) in university hospital high-care settings or (III) general health care

Locations (3)

University Hospital Wuerzburg
Würzburg, Bavaria, Germany
University Hospital Schleswig-Holstein, Campus Kiel
Kiel, Schleswig-Holstein, Germany
University Hospital Charité Berlin
Berlin, Germany