COVID-19 Registry Rhineland-Palatinate (Germany)
- Conditions
- COVID
- Interventions
- Other: Prospective oberservational registry
- Registration Number
- NCT04335188
- Lead Sponsor
- IHF GmbH - Institut für Herzinfarktforschung
- Brief Summary
Documentation of all patients undergoing inpatient treatment for SARS-CoV-2 infection with regard to clinical status at admission, medical history, inpatient treatment and course of disease. The aim is to create a risk stratification of the infection on the basis of clinical data as well as therapy and disease progression of the patients. This may also contribute to a better planning of resources.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 2589
- In-patients fulfilling the following criteria:
SARS-CoV-2 infection In-patient treatment Written informed consent for participation in observational study
- No explicit medical exclusion criteria are stated to avoid selection bias.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description In-patients with SARS-CoV-2 infection Prospective oberservational registry In-patients fulfilling the following criteria: SARS-CoV-2 infection In-patient treatment Written informed consent for participation in observational study No explicit medical exclusion criteria are stated to avoid selection bias.
- Primary Outcome Measures
Name Time Method Chest CT throughout study completion, in average 1.5 years presence of infiltrates
Chest x-ray throughout study completion, in average 1.5 years presence of infiltrates
Medication throughout study completion, in average 1.5 years number of patients with medication changes
Supportive care - ICU throughout study completion, in average 1.5 years number of patients with ICU treatment required
Intra-hospital complications throughout study completion, in average 1.5 years number of patients with complications during hospital stay
Supportive care - oxygen therapy throughout study completion, in average 1.5 years number of patients with oxygen therapy required
Therapeutic strategies throughout study completion, in average 1.5 years number of patients with ECMO required
Supportive care - ventilation throughout study completion, in average 1.5 years number of patients with ventilation required
Lab parameters throughout study completion, in average 1.5 years number of patients with significant changes in lab parameters
Vital status at discharge throughout study completion, in average 1.5 years vital status at discharge: alive, dead
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Klinikum der Stadt Ludwigshafen am Rhein GmbH, Klinik für Herzchirurgie
🇩🇪Ludwigshafen, RLP, Germany