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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT04357028
Other study ID # N-30-2020
Secondary ID
Status Suspended
Phase Phase 3
First received
Last updated
Start date July 13, 2020
Est. completion date January 1, 2021

Study information

Verified date December 2020
Source Kasr El Aini Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Till now, mortality reports among children below 9 years remains extremely low despite that the incidence of death toll is high and exceeding 50,000 patients among older population, One speculation for lower SARS infectivity is that cross-protective antibodies against measles vaccine ( MV). In mice susceptible to measles virus, recombinant MV induced the highest titers of neutralizing antibodies and fully protected immunized animals from intranasal infectious challenge with SARS-CoV, The primary objective of the present study is to determine the benefit of measles vaccine in health care professional to decrease the incidence of COVID-19. We Hypothesized that, measles vaccine may lower the incidence of serologically proven SARS-CoV-2 infection and reported respiratory illness


Recruitment information / eligibility

Status Suspended
Enrollment 200
Est. completion date January 1, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Age 18-50 years old - Subjects who are willing to comply with the requirements of the study protocol and scheduled visits (for example, completion of the subject diary, return for follow-up visits) and who are willing to make themselves available for the duration of the study with access to a consistent means of telephone contact Exclusion Criteria: - acute severe illness - recent receipt of a blood product - history of thrombocytopenia - Pregnant females - any chronic medical condition - Any participant receiving any immune suppressive medication - Immunocompromised staff - Participants who have egg allergy - Participants who care for immune compromised hosts - Participants who test positive for COVID-19 serology prior to randomization

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Measles-Mumps-Rubella Vaccine
Measles mumps Rubella vaccine is a weak attenuated life vaccine
Placebos
0.5 ml subcutaneous of saline will be injected in posterior triceps aspect of upper arm

Locations

Country Name City State
Egypt Cairo University Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Kasr El Aini Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary COVID-19 disease incidence Number of participants with asymptomatic or mild COVID-19 disease defined as fever (using self-reported questionnaire), plus at least one sign or symptom of respiratory disease including cough, runny/blocked nose (using self-reported questionnaire), plus positive SARS-Cov-2 test (PCR or serology) Time Frame: Measured over the 6 months following randomization
Secondary SARS-CoV-2 pneumonia Number of pneumonia cases (abnormal chest X-ray) (using self-reported questionnaire and/or medical/hospital records) associated with a positive SARS-CoV-2 test Time Frame: Measured over the 6 months following randomization
Secondary Critical care admission duration with SARS-CoV-2 Number of days admitted to critical care (using self-reported questionnaire and/or medical/hospital records) associated with a positive SARS-CoV-2 test Time Frame: Measured over the 6 months following randomization
Secondary Oxygen therapy with SARS-CoV-2 Need for oxygen therapy (using self-reported questionnaire and/or medical/hospital records) associated with a positive SARS-CoV-2 test Time Frame: Measured over the 6 months following randomization
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