Actively Recruiting
Is a Third Dose of MMRV Vaccine Beneficial for the Adult Population in Alberta?
Led by University of Alberta · Updated on 2026-03-16
200
Participants Needed
1
Research Sites
150 weeks
Total Duration
On this page
Sponsors
U
University of Alberta
Lead Sponsor
M
Merck Canada Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
The current recommendation for a full course of measles-mumps-rubella-(varicella) vaccine (MMR(V)) is two doses. The problem is, many individuals within the vaccinated cohort show antibody levels that are below the level considered to be protective, even after two doses of vaccine. Because of these waning antibody levels, it is currently unknown whether highly vaccinated populations are protected from infection against measles, mumps, rubella, or varicella should they be exposed to any of these viruses. The uncertainty of a woman's immune status is partly due to the type of testing that is used to indicate protection. While immunity to viral infection requires both a humoral and a cell mediated immune (CMI) response, only humoral (antibody) responses are measured routinely in the laboratory. This study will examine CMI responses and the role of a third dose of vaccine for previously vaccinated women whose antibody levels are below the cut off. This study will not administer vaccine, but rather will include women who have received a third dose of vaccination through routine health care follow up in the study cohort.
CONDITIONS
Official Title
Is a Third Dose of MMRV Vaccine Beneficial for the Adult Population in Alberta?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women who are pregnant and have undergone routine prenatal screening for rubella antibodies.
You will not qualify if you...
- Women younger than 18 years of age
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Alberta
Edmonton, Alberta, Canada, T6G2R3
Actively Recruiting
Research Team
C
Carmen Charlton, PhD
CONTACT
M
Michael H Mengel
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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