Trials / Completed
CompletedNCT04854837
Safety of Remdesivir Treatment in COVID-19 Patients Requiring Hemodialysis
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 45 (actual)
- Sponsor
- Semmelweis University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The FDA approved the antiviral drug remdesivir for use in adults for the treatment of COVID-19 requiring hospitalization. There are only limited data about the safety of the drug in hemodialysed patents. Chronic kidney disease is a risk factor in COVID-19 for developing severe disease. The aim of our investigation is to observe the safety of remdesivir among hemodialysed patients requiring hospitalization for COVID-19. We are going to compare two group's data: 1. Hemodialysed COVID-19 patients requiring hospitalization because of pneumonia and need of oxygen supplementation, and admitted after 12/Apr/2021 - these patients received remdesivir. 2. Hemodialysed COVID-19 patients requiring hospitalization because of pneumonia and need of oxygen supplementation, and admitted before 12/Apr/2021 - these patients did not receive remdesivir.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Remdesivir | Remdesivir treatment |
Timeline
- Start date
- 2021-04-12
- Primary completion
- 2022-09-30
- Completion
- 2022-09-30
- First posted
- 2021-04-22
- Last updated
- 2022-11-09
Locations
1 site across 1 country: Hungary
Source: ClinicalTrials.gov record NCT04854837. Inclusion in this directory is not an endorsement.