G93.3
Conditions
Interventions
Group 1: This is a cohort study: a registry will be set up to enrol consecutive patients after acute COVID-19 disease or other infections who have persistent symptoms in the sense of a post-acute infe
Sponsors
Universitätsklinikum Heidelberg, Abteilung Allgemeinmedizin und Versorgungsforschung
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The prospective analysis from the date of approval will include all consenting patients who have had SARS-CoV-2 infection or any other infection consistent with the symptoms leading to presentation and who give written consent to be included in the study.
Exclusion criteria
Exclusion criteria: Lack of legal capacity, lack of consent, execution of sentence, patients < 18 years of age.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To establish a registry in which patients with persistent symptoms of post-acute infection syndrome after acute COVID-19 disease or other infections will be consecutively enrolled. The primary objective of the study is to characterize patients with regard to the long-term consequences of the post-acute infection syndrome by recording patient self-assessments using questionnaires and clinical and laboratory parameters. | — |
Secondary
| Measure | Time frame |
|---|---|
| Follow-up of patients as part of medically indicated follow-up examinations (either as part of re-admissions) or as part of written follow-up surveys to record the course of the disease, (experience of) use, factors influencing the course of the disease and the development of long-term sequelae. | — |
Countries
Germany
Contacts
Public ContactSandra Stengel
Universitätsklinikum Heidelberg, Abteilung Allgemeinmedizin und Versorgungsforschung
Outcome results
None listed