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Measles Vaccine in HCW

Effectiveness of Measles Vaccine in Health Care Professionals During COVID-19 Outbreak (Randomized Controlled Trial)

Status
Suspended
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04357028
Acronym
MV-COVID19
Enrollment
200
Registered
2020-04-22
Start date
2020-07-13
Completion date
2021-01-01
Last updated
2020-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19

Keywords

MMR vaccine, Respiratory failure,

Brief 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

Interventions

Measles mumps Rubella vaccine is a weak attenuated life vaccine

DRUGPlacebos

0.5 ml subcutaneous of saline will be injected in posterior triceps aspect of upper arm

Sponsors

Kasr El Aini Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
COVID-19 disease incidenceTime Frame: Measured over the 6 months following randomizationNumber 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)

Secondary

MeasureTime frameDescription
SARS-CoV-2 pneumoniaTime Frame: Measured over the 6 months following randomizationNumber of pneumonia cases (abnormal chest X-ray) (using self-reported questionnaire and/or medical/hospital records) associated with a positive SARS-CoV-2 test
Critical care admission duration with SARS-CoV-2Time Frame: Measured over the 6 months following randomizationNumber of days admitted to critical care (using self-reported questionnaire and/or medical/hospital records) associated with a positive SARS-CoV-2 test
Oxygen therapy with SARS-CoV-2Time Frame: Measured over the 6 months following randomizationNeed for oxygen therapy (using self-reported questionnaire and/or medical/hospital records) associated with a positive SARS-CoV-2 test

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026