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Clinical Trials/NCT04527497
NCT04527497
Completed
Not Applicable

Clinical Course and Treatment of COVID-19 Inpatients in Hospital

Wissenschaftliches Institut Bethanien e.V1 site in 1 country35 target enrollmentAugust 1, 2020
ConditionsCOVID-19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
Wissenschaftliches Institut Bethanien e.V
Enrollment
35
Locations
1
Primary Endpoint
convalescence/death
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The study is an epidemiological observational study. It serves to collect data from patients with positive COVID-19 test results who are hospitalized. All data describing the course of the inpatient stay are recorded (Length of stay, course of therapy, medication, X-ray and CT results,ventilation mode and duration, laboratory). Furthermore, anthropometric data and information on COVID-19 symptoms is recorded.

Detailed Description

The aim of this study is to describe the course of disease and the treatment of patients suffering from COVID-19 who are hospitalized and treated as inpatients: 1. Are there common features (previous illnesses, medication, age, BMI, etc.), which may influence the course of disease? 2. Are there therapeutic procedures that have a positive or negative impact on the course of the disease or the length of stay in the intensive care unit/ the duration of ventilation (early/late intubation, CPAP, NIV, ECMO)?

Registry
clinicaltrials.gov
Start Date
August 1, 2020
End Date
August 31, 2021
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Wissenschaftliches Institut Bethanien e.V
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • positive COVID-19 test result
  • Age \> 18 years

Exclusion Criteria

  • Age \< 18 years
  • negative COVID-19 test result
  • lack of agreement
  • Any medical, psychological or other condition, that restricts the ability of the person to be informed and to give the consent for voluntary participation in this trial

Outcomes

Primary Outcomes

convalescence/death

Time Frame: through study completion, an average of 2 months

has patient died or has patient recovered

Secondary Outcomes

  • length of stay in hospital(through study completion, an average of 2 months)
  • length of stay in the intensive care unit(through study completion, an average of 2 months)

Study Sites (1)

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