Clinical Trials Directory

Trials / Unknown

UnknownNCT04347278

Observational Study of Follow-up of Hospitalized Patients Diagnosed With COVID-19 to Evaluate the Effectiveness of the Drug Treatment Used to Treat This Disease. COVID-19 Registry

Status
Unknown
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Instituto de Investigación Marqués de Valdecilla · Academic / Other
Sex
All
Age
1 Year – 100 Years
Healthy volunteers
Not accepted

Summary

The infection caused by COVID19 worldwide makes it necessary to monitor drugs administered for the treatment of patients hospitalized with SARS-CoV-2. In order to know more about the efficacy and safety of the treatments used, researchers from the Cantabrian health service have developed an observational study, in the form of an ambispective registry, in which clinical data from patients treated with the different drugs currently recommended by the Spanish Agency of Medicines and Health Products (SAMHP) and the Ministry of Health, or others that may arise, are collected and analyzed. Although the conduct of clinical trials is a priority at this time, we cannot lose the clinical experience that is currently being generated, which may allow us to improve the therapeutic strategies for future patients.

Conditions

Interventions

TypeNameDescription
DRUGPatients with the treatment agains COVID19Data will be collected from patients who receive any of the treatments included in the "Technical Document. Manejo clínico del COVID-19: tratamiento médico" of the Ministry of Health, and "Tratamientos disponibles para el manejo de la infección respiratoria por SARS-CoV-2" of the AEMPS, either as antivirals or as treatment of the inflammatory process in patients with SARS, or others as they arise.

Timeline

Start date
2020-04-22
Primary completion
2021-10-15
Completion
2022-01-01
First posted
2020-04-15
Last updated
2021-09-16

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04347278. Inclusion in this directory is not an endorsement.