CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


BCG-DenmarkWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug2176 Saline Wiki 0.38

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
D055371 Acute Lung Injury NIH 0.10
D012127 Respiratory Distress Syndrome, Newborn NIH 0.10
D012128 Respiratory Distress Syndrome, Adult NIH 0.09
D011014 Pneumonia NIH 0.06

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.06

There is one clinical trial.

Clinical Trials


1 Using BCG Vaccine to Enhance Non-specific Protection of Health Care Workers During the COVID-19 Pandemic. A Randomized Controlled Multi-center Trial

Background: The COVID-19 pandemic challenges the available hospital capacity, and this will be augmented by absenteeism of healthcare workers (HCW). HCW are at high risk, currently HCW constitute 20% of all the COVID-19 cases in Denmark. Strategies to prevent absenteeism of HCW are urgently needed. Bacille Calmette-Guérin (BCG) is a vaccine against tuberculosis, with protective non-specific effects against other infections; significant reductions in morbidity and mortality have been reported, and a plausible immunological mechanism has been identified. We hypothesize that BCG vaccination can reduce HCW absenteeism during the COVID-19 pandemic. Primary objective: To reduce absenteeism among HCW with direct patient contacts during the COVID-19 epidemic. Secondary objective: To reduce the number of HCW that are infected with SARS-CoV-2 during the COVID-19 epidemic and to reduce the number of hospital admissions amongst HCW with direct patient contacts during the COVID-19 epidemic. Study design: A multi-center randomized placebo controlled trial. Study population: 1500 HCW with direct patient contacts; defined as nurses, physicians and other medical staff working at emergency rooms and wards where COVID-infected patients are treated. Intervention: Participants will be randomized 1:1 to intradermal administration of a standard dose of BCG vaccine or placebo (saline). Main study parameters/endpoints: Primary endpoint: Number of days of (unplanned) absenteeism for any reason. Secondary endpoints: Number of days of (unplanned) absenteeism because of documented COVID infection. Cumulative incidence of hospital admissions. Risk for participants and impact: Based on previous experience and randomized controlled trials in adult and elderly individuals, the risks of BCG vaccination are considered low. The objective of this trial is to evaluate the potential beneficial effects of BCG vaccination through a lower work absenteeism rate of HCW and/or a mitigated clinical course of COVID infection.

NCT04373291 COVID-19 Non-specific Effects of Vaccines Morbidity Absenteeism Heterologous Immunity Biological: BCG-Denmark Biological: Saline

Primary Outcomes

Measure: Number of days of unplanned absenteeism for any reason

Time: 6 months

Secondary Outcomes

Measure: The cumulative incidence of documented COVID

Time: 6 months

Measure: The cumulative incidence of hospital admission for any reason

Time: 6 months

Measure: The number of days of unplanned absenteeism, because of documented COVID

Time: 6 months

Measure: The number of days of absenteeism, because of imposed quarantine as a result of exposure to SARS-CoV-2

Time: 6 months

Measure: The number of days of absenteeism, because of imposed quarantine as a result of having acute respiratory symptoms, fever or documented SARS- CoV-2 infection

Time: 6 months

Measure: The number of days of unplanned absenteeism because of self-reported acute respiratory symptoms

Time: 6 months

Measure: The number of days of self-reported fever (≥38 °C)

Time: 6 months

Measure: The number of days of self-reported acute respiratory symptoms

Time: 6 months

Measure: The cumulative incidence of self-reported acute respiratory symptoms

Time: 6 months

Measure: The cumulative incidence of death for any reason

Time: 6 months

Measure: The cumulative incidence of death due to documented COVID

Time: 6 months

Measure: The cumulative incidence of Intensive Care Admission for any reason

Time: 6 months

Measure: The cumulative incidence of Intensive Care Admission due to documented COVID

Time: 6 months

Measure: The cumulative incidence of Hospital Admission due to documented COVID

Time: 6 months


No related HPO nodes (Using clinical trials)