Clinical Trials Logo

Sars-CoV2 clinical trials

View clinical trials related to Sars-CoV2.

Filter by:

NCT ID: NCT04385810 Completed - Covid19 Clinical Trials

Description of Ophthalmologic Injuries in Intensive Care During the SARS-CoV2 Epidemic - COVID19

DOCOV
Start date: April 27, 2020
Phase: N/A
Study type: Interventional

The management of patients with SARS-CoV2 in respiratory distress can expose to corneal or retinal lesions induced by the stay in intensive care. Examination by ophthalmologists would make it possible to detect the most of the ophthalmologic problems known in intensive care and to provide an early, preventive or curative therapeutic response when possible, in order to avoid irreversible visual loss. The object of the research is to assess the presence and the importance of surface ophthalmologic lesions, the presence and the importance of retinal or optic nerve lesions, in order to improve the monitoring and primary prevention of this population

NCT ID: NCT04385212 Completed - Clinical trials for Coronavirus Infection

Outcomes in Hospitalized Older Patients With COVID-19

Start date: March 13, 2020
Phase:
Study type: Observational

In December 2019, the first patients infected with the 2019 novel coronavirus (2019-nCoV) were diagnosed in Wuhan. The clinical presentation and course of Severe Acute Respiratory Syndrome-CoV-2 (SARS-CoV-2) infection is poorly understood in older patients and is certainly different from the general population. This project is designed to better understand and to determine clinical, biological and radiological markers of poor adverse outcomes in hospitalized older patients diagnosed with COVID-19.

NCT ID: NCT04382547 Completed - Covid-19 Clinical Trials

Treatment of Covid-19 Associated Pneumonia With Allogenic Pooled Olfactory Mucosa-derived Mesenchymal Stem Cells

Start date: May 11, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Treatment of patients with Covid-19 associated pneumonia using intravenous injection of allogenic pooled olfactory mucosa-derived mesenchymal stem cells

NCT ID: NCT04381364 Active, not recruiting - Covid-19 Clinical Trials

Inhalation of Ciclesonide for Patients With COVID-19: A Randomised Open Treatment Study (HALT COVID-19)

HALT
Start date: May 29, 2020
Phase: Phase 2
Study type: Interventional

Randomized open label clinical trial carried out at study centers in Sweden, including Karolinska University Hospital, S:t Göran Hospital, Danderyd Hospital and Västmanlands Hospital. Patients with COVID-19 who are hospitalized with oxygen therapy are eligible for inclusion. Subjects are randomized to 14 days of inhalation with ciclesonide 360 µg twice daily or to standard of care. Primary outcome is duration of received supplemental oxygen therapy. Key secondary outcome is a composite outcome of death and received invasive mechanical ventilation within 30 days.

NCT ID: NCT04379492 Withdrawn - COVID-19 Clinical Trials

A Study of Hydroxycholoroquine Compared to Placebo as Treatment for People With COVID-19

Start date: May 5, 2020
Phase: Phase 2
Study type: Interventional

This study is being done to see if hydroxychloroquine is an effective treatment for COVID-19.

NCT ID: NCT04379336 Completed - COVID-19 Clinical Trials

BCG Vaccination for Healthcare Workers in COVID-19 Pandemic

Start date: May 4, 2020
Phase: Phase 3
Study type: Interventional

A novel betacoronavirus, SARS-CoV-2, is spreading rapidly throughout the world. A large epidemic in South Africa may overwhelm available hospital capacity and healthcare resources which would be worsened by absenteeism of healthcare workers and other frontline staff (HCW). Strategies to prevent morbidity and mortality of HCW are desperately needed to safeguard continuous patient care. Bacillus Calmette-Guérin (BCG) is a vaccine against tuberculosis (TB), with protective non-specific effects against other respiratory tract infections in in vitro and in vivo studies, with reported morbidity and mortality reductions as high as 70%. We hypothesize that a BCG vaccination may reduce the morbidity and mortality of healthcare workers during the COVID-19 outbreak in South Africa.

NCT ID: NCT04378842 Completed - Critical Illness Clinical Trials

COVID-19 and ICU-acquired MDR Bacteria

COVID-BMR
Start date: May 18, 2020
Phase:
Study type: Observational

This multicenter before-after study aimed to determine the impact of infection related to SARS-CoV-2 on the incidence of ICU-acquired multidrug resistant (MDR) bacteria.

NCT ID: NCT04377646 Not yet recruiting - COVID19 Clinical Trials

A Study of Hydroxychloroquine and Zinc in the Prevention of COVID-19 Infection in Military Healthcare Workers

COVID-Milit
Start date: May 4, 2020
Phase: Phase 3
Study type: Interventional

A multicenter randomized clinical trial aiming to assess the efficacy of hydroxychloroquine associated to Zinc compared to hydroxychloroquine, in the prevention of Military Health Professionals Exposed to SARS CoV2 in Tunisia

NCT ID: NCT04374617 Completed - COVID-19 Clinical Trials

Risk of Venous Thromboembolism in Critically Ill Patients With Severe COVID-19

Start date: April 1, 2020
Phase:
Study type: Observational

Severe COVID-19 patients at a high risk of venous thromboembolism. We studied patients in 2 intensive care units of university hospitals in Barcelona and Badalona, Spain. We performed a cut-off screening of deep venous thrombosis (DVT) with bilateral duplex ultrasound to 230 patients.

NCT ID: NCT04374019 Terminated - COVID Clinical Trials

Novel Agents for Treatment of High-risk COVID-19 Positive Patients

Start date: May 1, 2020
Phase: Phase 2
Study type: Interventional

This is a multi-arm, phase II trial for rapid efficacy and toxicity assessment of multiple therapies immediately after COVID19 positive testing in high-risk individuals. Therapies include stand-alone or combination treatment with hydroxychloroquine, azithromycin, ivermectin, or camostat mesilate, artemesia annua. The hypothesis of this study is that the addition of agents that inhibit viral entry or replication of SARS-CoV-2 virus replication in will be devoid of additional moderate to severe toxicities, will prevent clinical deterioration, and will improve viral clearance in high risk individuals.