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Covid19 clinical trials

View clinical trials related to Covid19.

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NCT ID: NCT04380961 Completed - Clinical trials for Critical Confirmed Coronavirus Disease (COVID)-19

A Study to Evaluate the Efficacy and Safety of Sirukumab in Confirmed Severe or Critical Confirmed Coronavirus Disease (COVID)-19

Start date: April 24, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the clinical response of sirukumab (administered as a single intravenous dose) plus standard of care (SOC) compared to placebo plus SOC in COVID-19.

NCT ID: NCT04380896 Completed - Clinical trials for SARS-CoV-2 Infection

COVID-19 Staff Testing of Antibody Responses Study (Co-Stars)

Co-Stars
Start date: April 27, 2020
Phase:
Study type: Observational

This study will perform prospective repeated serological antibody testing on a cohort of at least 1000 healthcare workers at Great Ormond Street Hospital. Within this cohort, a subset of 150-250 staff members with confirmed (PCR positive) SARS-CoV-2 disease will be followed with intensive monthly testing for 6 months to determine whether antibody levels in the blood are maintained or decrease during this time. All 1000 recruited healthcare workers will be followed 6-monthly

NCT ID: NCT04380792 Completed - COVID-19 Clinical Trials

Prevalence of DVT or PE in Patients Infected With COVID-19 Admitted to Hospital

SCREENING
Start date: April 13, 2020
Phase:
Study type: Observational

The main objectives are: - To establish the prevalence of deep venous thrombosis through ultrasonography in Patients infected with COVID-19 admitted to hospital. - To identify patients with higher risk of deep venous thrombosis.

NCT ID: NCT04380779 Completed - COVID-19 Clinical Trials

Prevalence of Severe Bleeding in COVID-19 Patients Treated With Higher Than Recommended Thromboprophylaxis Doses

BLEEDING
Start date: April 13, 2020
Phase:
Study type: Observational

The main objectives are: - To establish the prevalence of major bleeding in patients treated with higher than recommended thromboprophylaxis doses. - To identify variables associated to higher risk of bleeding.

NCT ID: NCT04380727 Completed - COVID-19 Clinical Trials

Almitrine and COVID-19 Related Hypoxemia

Start date: March 20, 2020
Phase:
Study type: Observational [Patient Registry]

In severe COVID-19 pulmonary failure, the profound hypoxemia is mainly related to pulmonary vasodilation with altered hypoxic pulmonary vasoconstriction (HPV). Besides prone positioning, other non-ventilatory strategies may reduce the intrapulmonary shunt. This study has investigated almitrine, a pharmacological option used in standard care to improve oxygenation. A case control series of mechanically ventilated confirmed COVID-19 patients was recorded. At stable ventilatory settings, consecutive patients received two doses of almitrine (4 and 12 mcg/kg/min) at 30-45 min interval each, and were compared to 7 "control" COVID-matched patients conventionally treated. The end-point was the reduction of intra-pulmonary shunt, with an increase in partial pressure of arterial oxygen (PaO2) and central venous oxygen saturation (ScvO2).

NCT ID: NCT04380714 Completed - COVID-19 Clinical Trials

Changes in the Consumption of Psychoactive Substances During Containment Linked to COVID-19

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

The SARS-CoV 2 pandemic started in China in December 2019, then reached France on January 24, 2020. On March 14, France moved into phase 3 of the epidemic threshold with the implementation of containment measures on March 17 Measures were put in place by N.Belloubet (French Minister of Justice) from March 17, including suspension of visiting rooms and activities in detention. Containment provides boredom and isolation with many potential consequences: sleep disturbance, anxiety, PTSD, depression, suicide, addictive behavior and violence. However,prisoners have a higher prevalence of substance use disorders than the general population. What will have been the impact of the confinement on the consumption of psychoactive substances by prisoners at the Villeneuve Les Maguelone prison. - Anonymous questionnaire from the start - Collection of socio-demographic data - Collection of consumption data before and during containment - Collection of monitoring data

NCT ID: NCT04380688 Completed - COVID-19 Clinical Trials

Acalabrutinib Study With Best Supportive Care Versus Best Supportive Care in Subjects Hospitalized With COVID-19.

CALAVI US
Start date: June 13, 2020
Phase: Phase 2
Study type: Interventional

CALAVI US will investigate the safety, efficacy and pharmacokinetics of acalabrutinib together with Best Supportive Care in the treatment of COVID-19.

NCT ID: NCT04380519 Completed - COVID-19 Clinical Trials

Study of the Efficacy and Safety of a Single Administration of Olokizumab and RPH-104 With Standard Therapy in Patients With Severe Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection (COVID-19)

Start date: April 23, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective of the study was to evaluate the efficacy and safety of a single dose of RPH-104 (80 mg) or OKZ (64 mg) compared to placebo in addition to standard therapy in patients with severe SARS-CoV-2 infection (COVID-19) at Day 15 of the study.

NCT ID: NCT04379661 Completed - COVID-19 Clinical Trials

SUNLIGHT Study: Online Support Groups for MS to Address COVID-19

Start date: May 7, 2020
Phase: N/A
Study type: Interventional

Stress and anxiety can have an adverse impact on health, and the experience of many around the 2020 outbreak of COVID-19 is affecting health and well-being. Individuals with chronic disease such as multiple sclerosis may be particularly vulnerable in some ways, but also particularly resilient in others. This study evaluates the effects of belonging to online support groups that meet weekly for 12 weeks to address the stress and anxiety felt by individuals with Multiple Sclerosis (MS). This study will also measure and explore the effects of online support groups.

NCT ID: NCT04379544 Completed - Respiratory Failure Clinical Trials

Prognostic Value of Point of Care Cardiac and Lung Ultrasound in COVID-19

CLUSCO
Start date: April 23, 2020
Phase:
Study type: Observational [Patient Registry]

This is a protocol-driven observational study of lung ultrasound and focused echocardiography images obtained in the Emergency Department (ED) and Intensive Care Unit (ICU) settings as a part of existing standard of care. The objectives of this study are as follows: 1. To characterize various clinical and cardiopulmonary ultrasound findings and describe their relationship with the clinical course of patients with COVID-19 in the ED and ICU. 2. To describe, develop, and validate a prediction tool that can accurately predict the need for invasive mechanical ventilation (IMV) and acute respiratory failure in COVID-19 patients using clinical, laboratory, and ultrasound data.