Clinical Trial to Evaluate the Efficacy of Different Treatments in Patients With COVID-19
- Conditions
- SARS-CoV-2 Infection
- Interventions
- Drug: Emtricitabine/Tenofovir Disoproxil Fumarate 200 MG-245 MG Oral Tablet [TRUVADA]
- Registration Number
- NCT04890626
- Brief Summary
Currently COVID-19 is an international public health emergency. Most COVID-19 patients have mild or uncomplicated disease, but approximately 14% develop severe disease that requires hospitalization and oxygen therapy, and up to 5% of patients require admission to Intensive Care Units.
To date, the only treatments that have shown efficacy in a clinical trial are remdesivir and dexamethasone. The main objective is to provide reliable estimates on the effects of different treatment strategies on the outcome and mortality of patients with SARS-CoV-2 infection.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 356
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Rescue randomization: Arm: Dexamethasone + Baricitinib Baricitinib + dexamethasone Rescue randomization: patients with oxygen requirements, O2 Sat \<95% at any time, and at least one of the following inflammation markers: IL-6, CRP, D-dimer, LDH or ferritin above the upper limit of the normal range. Arms: Dexamethasone + Baricitinib or Dexamethasone. Main randomization.Arm: Emtricitabine / Tenofovir disoproxil fumarate Emtricitabine/Tenofovir Disoproxil Fumarate 200 MG-245 MG Oral Tablet [TRUVADA] Emtricitabine / Tenofovir disoproxil fumarate Rescue randomization: Arm: Dexamethasone Dexamethasone Rescue randomization: patients with oxygen requirements, O2 Sat \<95% at any time, and at least one of the following inflammation markers: IL-6, CRP, D-dimer, LDH or ferritin above the upper limit of the normal range. Arms: Dexamethasone + Baricitinib or Dexamethasone.
- Primary Outcome Measures
Name Time Method Mortality at 28 days
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hospital Universitario La Paz
🇪🇸Madrid, Spain