Response of Older Adults to Influenza Vaccination With Regard to Cytomegalovirus (CMV) Status (CMVflu)
Primary Purpose
Influenza
Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Fluarix
Sponsored by
About this trial
This is an interventional prevention trial for Influenza focused on measuring Influenza Vaccine, CMV
Eligibility Criteria
Inclusion Criteria:
- No contraindications to vaccination as specified in the "Green Book" - Immunisation Against Infectious Disease, HMSO.
- Written informed consent obtained
- Subject aged no less than 50 years 0 days and no older than 79 years and 364 days at enrollment.
Sites / Locations
- Hertfordshire Primary Care Trust
Outcomes
Primary Outcome Measures
Response to influenza vaccination (HI)
Secondary Outcome Measures
Full Information
NCT ID
NCT00442975
First Posted
March 2, 2007
Last Updated
August 28, 2018
Sponsor
Public Health England
Collaborators
Royal Free and University College Medical School
1. Study Identification
Unique Protocol Identification Number
NCT00442975
Brief Title
Response of Older Adults to Influenza Vaccination With Regard to Cytomegalovirus (CMV) Status
Acronym
CMVflu
Official Title
A Phase IV, Single Group Study to Evaluate the Immune Response to Licensed Seasonal Influenza Vaccine and Relationship of This to Cytomegalovirus-associated Immunosenescence in UK Older Adults Aged 50-80 Years
Study Type
Interventional
2. Study Status
Record Verification Date
February 2008
Overall Recruitment Status
Completed
Study Start Date
March 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Public Health England
Collaborators
Royal Free and University College Medical School
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study is being undertaken to evaluate responses to seasonal influenza vaccine in older adults with respect to their CMV status. CMV is cytomegalovirus and is an organism that infects many people, but does not usually cause disease in the individual unless they are immunocompromised i.e. their immune system is not working well such as in the case of HIV infection. CMV is believed to have infected up to 80% of individuals in the age group we will be looking at in our study and we are interested in whether this infection affects their responses to vaccination.
Detailed Description
Human cytomegalovirus (HCMV) is an important pathogen or disease-causing virus, which can result in disease in the unborn child as well as in individuals whose immune systems are not working properly such as those with HIV or who are receiving some treatments for cancer, where the body's ability to fight infection is not as good as in healthy people. HCMV infects the majority of the population, yet rarely causes overt disease which would limit the capacity of the host to transmit HCMV to others. This virus is thought to be millions of years old and because of this we think that it has evolved over time to become very efficient at evading the immune system. This means it has become very efficient at moving through the human population and resulting in humans devoting more immunological resources to controlling this virus than to any other. Recent studies have reported that the immune system does work less efficiently in older people, especially in elderly patients with CMV antibodies compared to age matched controls who did not have CMV antibodies.
It is well recognized that responses to vaccination are generally lower in older populations compared to children, so they may be thought to be immunologically in a suboptimal position. It is proposed that this may be as a result of diversion of key factors in the immune system to address CMV infection, the incidence of which increases with age. This study will allow assessment of responses to licensed seasonal influenza vaccine with respect to age and CMV status and will provide baseline information as a proof of principle on which a larger study will be designed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza
Keywords
Influenza Vaccine, CMV
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Biological
Intervention Name(s)
Fluarix
Primary Outcome Measure Information:
Title
Response to influenza vaccination (HI)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
No contraindications to vaccination as specified in the "Green Book" - Immunisation Against Infectious Disease, HMSO.
Written informed consent obtained
Subject aged no less than 50 years 0 days and no older than 79 years and 364 days at enrollment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth Miller, MBBS FRCPath
Organizational Affiliation
Public Health England
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hertfordshire Primary Care Trust
City
Stevenage
Country
United Kingdom
12. IPD Sharing Statement
Learn more about this trial
Response of Older Adults to Influenza Vaccination With Regard to Cytomegalovirus (CMV) Status
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