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Covid19 clinical trials

View clinical trials related to Covid19.

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NCT ID: NCT05639465 Recruiting - Coping Skills Clinical Trials

Intervention to Prevent Behavioral Health Symptoms Among Pandemic Affected Children

Start date: November 15, 2022
Phase: N/A
Study type: Interventional

Racial and ethnic minority children who live in socioeconomically disadvantaged communities are disproportionately impacted by pandemic and climate-induced disasters. Although effective interventions have been designed to treat mental health related symptoms in post-disaster settings, accessible, empirically supported prevention interventions are needed to prevent the onset of mental and behavioral health issues among these children. Building on our preliminary findings, the proposed study examines the efficacy and implementation of a COVID-19 adapted disaster focused prevention intervention, Journey of Hope-C19, in preventing behavioral health and interpersonal problems among racial and ethnic minority children who live in low-resource high poverty communities.

NCT ID: NCT05639205 Not yet recruiting - COVID-19 Clinical Trials

Shaping Care Home COVID-19 Testing Policy

VIVALDI-CT
Start date: December 2022
Phase: Phase 3
Study type: Interventional

The goal of this interventional study is to investigate whether continued use of regular asymptomatic testing in staff is a feasible, effective and cost-effective strategy to reduce the impact of COVID-19 in care homes. The trial aims to quantify the benefits and harms of regular asymptomatic testing in care home staff to inform policy. The rationale for regular asymptomatic testing is that it may reduce the risk of severe disease in residents and the frequency/severity of outbreaks. Participants (care home staff) will perform regular asymptomatic tests for Covid-19. Should they test positive they will be required to refrain from working and be provided with sick pay. Care providers will be reimbursed for the costs of employing agency staff to cover staff sickness absence that results directly from the trial.

NCT ID: NCT05639192 Recruiting - COVID-19 Clinical Trials

Asunercept for the Treatment of Patients With Moderate to Severe COVID-19 Disease

ASUCOV
Start date: November 3, 2022
Phase: Phase 3
Study type: Interventional

This clincial trial is a prospective, multicenter, randomized, double-blind, placebo-controlled Phase III trial in hospitalized patients with moderate to severe COVID-19 corresponding to score 5 or 6 on the WHO 10-point clinical progression scale (Grade 0-10). The investigational drug (APG101; International Nonproprietary Name: asunercept) will be given at a dose of 100 mg intravenously (i.v.) once weekly for a period of 4 weeks (1 dose each on d1, d8, d15, and d22) in addition to the treatment recommended by international, national, or local treatment guidelines (SoC) and will be compared with the control arm (i.e., SoC + placebo).

NCT ID: NCT05639166 Not yet recruiting - COVID-19 Clinical Trials

A Phase 2 Study in Adults to Assess the Safety and Efficacy of Inhaled IBIO123, for Post-exposure Prophylaxis of COVID-19

Start date: January 15, 2023
Phase: Phase 2
Study type: Interventional

This is a Phase 2, randomized, double-blind, multicentre, placebo-controlled study in adults to assess the safety and efficacy of inhaled IBIO123, for post-exposure prophylaxis of COVID-19. This study aims to evaluate the efficacy and the safety of IBIO123 and the prophylaxis effect of IBIO123 in participants exposed to COVID-19 in the setting of current and uninterrupted household contacts.

NCT ID: NCT05638932 Active, not recruiting - COVID-19 Clinical Trials

Methodologies for Observational Studies Comparing Inpatient COVID-19 Treatments

Start date: June 16, 2020
Phase:
Study type: Observational

To apply and compare two different methodological approaches (one applying diagnostics steps and contingencies and the other not) to the illustrative example described below: Illustrative Example - Objective I aims to characterize the risk of inpatient mortality [Primary Outcome] and progression to invasive mechanical ventilation (IMV) or extracorporeal membrane oxygenation (ECMO) [Secondary Outcome] up to 28 days after interleukin-6 receptor inhibitors (IL6Ri) or janus kinase inhibitor (JAKi) initiation among patients hospitalized with COVID-19 who initiate a corticosteroid of interest and require supplemental oxygen / non-invasive ventilation / high flow oxygen (O2/NIV/HFO) (but not IMV/ECMO). Illustrative Example - Objective II aims to characterize the risk of inpatient mortality [Primary Outcome] up to 28 days after IL6Ri or JAKi initiation among patients admitted to the ICU at hospital admission with COVID-19 who initiate a CSI and require IMV/ECMO. Hazard ratios (HR) and corresponding 95% confidence intervals (CI) will be estimated and reported for all outcome risks in Illustrative Example objectives.

NCT ID: NCT05638919 Not yet recruiting - COVID-19 Clinical Trials

Real World COVID-19 Antiviral Effectiveness Research

myRECOVER
Start date: December 6, 2022
Phase:
Study type: Observational

This study is a prospective observational cohort study to evaluate the benefit of oral antivirals (nirmatrelvir plus ritonavir or molnupiravir) in Ministry of Health institutions. In this study, we will observe the progress of COVID-19 study participants seen in the health clinic up to 90 days from their initial visit to the health clinic.

NCT ID: NCT05638724 Recruiting - Long COVID Clinical Trials

Munich Long COVID Registry Study for Children, Adolescents and Adults (MLC-R), COVID-19, SARS-CoV-2

MLC-R
Start date: July 20, 2022
Phase:
Study type: Observational [Patient Registry]

Long COVID refers to persistent symptoms after a generally mild acute COVID-19. Because the symptoms are often complex and vary from person to person, the term post-COVID syndrome is used synonymously. In the ICD-10 catalog, Long COVID is mapped as U09.9 as "post-COVID-19 conditions." Long COVID carries a high risk for chronic morbidity. This has serious consequences for individuals and society, especially when manifesting in young adulthood, adolescence, and childhood. Current data show that predominantly young women aged 30-40 years are affected by severe Long COVID. Despite only mild acute COVID-19, 10-15% of patients still show persistent symptoms six months later, including particularly frequently pathological exhaustion (fatigue), exercise intolerance with symptom worsening after exertion (so-called post-exertional malaise), neurocognitive complaints and circulatory disorders. In addition, general symptoms such as sleep disturbances, pain, or subfebrile temperatures have been described, as well as symptoms of all organ systems. In children and adolescents, less prevalence data are available to date. In initial studies, 4.4% and 4.6% of children and adolescents, respectively, show persistent symptoms after four weeks, 9.8% of 2-11 year olds and 13% of 12-16 year olds after five weeks, and 1.8% of children and adolescents with confirmed/probable SARS-CoV-2 infection after two months. Long COVID often results in impairment of daily life with limited ability to go to school or to work, up to and including inability to go to school or to work. Some patients manifest full-blown CFS, which has also been described after other viral infections, such as after glandular fever caused by Epstein-Bar virus (EBV). Similar to post-COVID CFS, CFS after primary EBV infection manifests predominantly in female adolescents and young adults. Whether it is the same severe, chronic disease despite similar clinical phenotype is uncertain. The mechanisms of pathogenesis of Long COVID and postinfectious CFS have been poorly elucidated. Initial studies of Long COVID suggest that autoimmunity, chronic inflammation, endothelial dysfunction, and psychosocial aspects contribute to pathogenesis. For postinfectious CFS, a causal interplay of genetic factors, stress, and infections has also been postulated, inducing a vicious cycle of dysregulation of the central and autonomic nervous system, immune defense, and metabolism.

NCT ID: NCT05638685 Completed - COVID-19 Clinical Trials

The Bodily Complaints Barometer: The Impact of the Corona Measures and of Contracting a COVID-19 Infection on the Body.

COVID-MSK
Start date: December 22, 2021
Phase:
Study type: Observational

Since December 2019, a new corona virus (SARS-CoV-2) causing COVID-19 disease, has expeditiously spread over the entire globe. Almost a half billion people caught the disease, and in those who survived, it soon became clear that residual complaints are not rare phenomena. Early focus lay on diminished lung capacity and cardiovascular-related problems. As time passed however, it became more apparent that those are not the only residual symptoms survivors may experience. Furthermore, nearly every country in the world took some sort of lockdown measures in order to try contain the spreading of the virus. These measures had great impact on all inhabitants, infected with the virus or not. This questionnaire-based study therefore aims to investigate (a) the effects of a COVID-19 infection on fatigue and/or musculoskeletal complaints, new or already existing, but also (b) the effects of lockdown measures on fatigue and/or musculoskeletal complaints, new or already existing, in people living, working or studying in Belgium during the pandemic.

NCT ID: NCT05638672 Not yet recruiting - COVID-19 Clinical Trials

COVID-19 Huashi Baidu Formula Clinical Study

Start date: December 15, 2022
Phase: N/A
Study type: Interventional

Combined with the regional and population characteristics of Asia and Africa, Huashi Baidu Granule was used to intervene in mild and ordinary patients with COVID-19, evaluate its efficacy and safety, and clarify its characteristics of action.

NCT ID: NCT05638633 Recruiting - Clinical trials for Post-COVID-19 Syndrome

Prednisolone and Vitamin B1/6/12 in Patients With Post-Covid-Syndrome

PreVitaCOV
Start date: November 11, 2022
Phase: Phase 3
Study type: Interventional

This is a multicenter, randomized, placebo controlled, double-blind phase III trial with four parallel groups studying studying the feasibility of RCT in primary care as well as the effectiveness of treatment with prednisolone and/or vitamin B1/6/12 for PC19S.