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Sars-CoV2 clinical trials

View clinical trials related to Sars-CoV2.

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NCT ID: NCT04351191 Terminated - Covid-19 Clinical Trials

PRophylaxis of Exposed COVID-19 Individuals With Mild Symptoms Using choloroquinE Compounds

PRECISE
Start date: April 15, 2020
Phase: Phase 4
Study type: Interventional

To treat Pakistani patients with non-life threatening symptomatic SARS-CoV-2 infection with an intent to reduce burden on institutional healthcare services by determining efficacy of different chloroquine and hydroxychloroquine dosing regimens in controlling SARS-CoV-2 infection.

NCT ID: NCT04347226 Terminated - Solid Tumor Clinical Trials

Anti-Interleukin-8 (Anti-IL-8) for Patients With COVID-19

Start date: April 16, 2020
Phase: Phase 2
Study type: Interventional

This study is for patients that are hospitalized for Coronavirus Disease 2019 (COVID-19). The purpose of this study is to see whether neutralizing interleukin-8 (IL-8) with BMS-986253 can help improve the health condition of participants infected with COVID-19. This is the first in-human study of this investigational product specifically in patients with severe COVID-19. Currently there are no FDA approved medications that improve the chance of survival in patients diagnosed with COVID-19. However there are usual treatments currently being used to help treat COVID-19 patients and BMS-986253 will be compared to these standard of care treatments in this study.

NCT ID: NCT04345848 Terminated - COVID Clinical Trials

Preventing COVID-19 Complications With Low- and High-dose Anticoagulation

COVID-HEP
Start date: April 28, 2020
Phase: Phase 3
Study type: Interventional

The ongoing COVID-19 pandemic affects millions of humans worldwide and has led to thousands of acute medical hospitalizations. There is evidence that hospitalized cases often suffer from an important infection-related coagulopathy and from elevated risks of thrombosis. Anticoagulants may have positive effects here, to reduce the burden of thrombotic disease and the hyperactivity of coagulation, and may also hold beneficial anti-inflammatory effects against sepsis and the development of ARDS. The investigators hypothesize that high-dose anticoagulants, compared with low-dose anticoagulants, lower the risk of venous and arterial thrombosis, disseminated intravascular coagulation (DIC) and mortality. This open-label controlled trial will randomize hospitalized adults with severe COVID-19 infection to therapeutic anticoagulation vs. thromboprophylaxis during the hospital stay.

NCT ID: NCT04327505 Terminated - COVID-19 Clinical Trials

Safety and Efficacy of Hyperbaric Oxygen for ARDS in Patients With COVID-19

COVID-19-HBO
Start date: June 3, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

COVID-19 may cause severe pneumonitis that require ventilatory support in some patients, the ICU mortality is as high as 62%. Hospitals do not have enough ICU beds to handle the demand and to date there is no effective cure. We explore a treatment administered in a randomized clinical trial that could prevent ICU admission and reduce mortality. The overall hypothesis to be evaluated is that HBO reduce mortality, increase hypoxia tolerance and prevent organ failure in patients with COVID19 pneumonitis by attenuating the inflammatory response.

NCT ID: NCT04320511 Terminated - COVID-19 Clinical Trials

Beaumont Quantitative Lung Function Imaging to Characterize Patients With SARS-COV 2

Start date: June 24, 2020
Phase:
Study type: Observational

The goal of this study is to evaluate if CT (Computerized Tomography) can effectively and accurately predict disease progression in patients with SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2). You may be eligible if you have been diagnosed with SARS-CoV-2, are an inpatient at Beaumont Hospital-Royal Oak and meet eligibility criteria. After consent and determination of eligibility, enrolled patients will have a CT scanning session. After the CT scan, patients are followed for 30 days by reviewing their medical records and by phone after discharge from hospital.