Complement 2: Blood Donations to Develop Vaccines Against Infectious Diseases
NCT ID: NCT01945307
Last Updated: 2023-04-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
101 participants
OBSERVATIONAL
2013-10-31
2023-03-31
Brief Summary
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The samples would be used in the laboratory analysis of clinical trials of vaccines used in adults and children, and some samples in pre-clinical (animal) experiments testing new vaccines before they enter human-stage testing. Most people have some form of protection against most bacteria already, so not everyone is a suitable blood donor for this laboratory test. We therefore start by taking a small blood sample and test this one before asking for more blood if we found yours suitable for the work we do.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Healthy adults
Healthy adults aged 18 to 70 years
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Aged between 18 and 70 years
* In good health as determined by medical history and clinical judgment of the Investigators
* Able to attend the scheduled visits and to comply with all study procedures
* If found to be a suitable complement that they are willing to be approached for further donations
Exclusion Criteria
* Have any known or suspected impairment or alteration of immune function, resulting from, as examples:congenital or acquired immunodeficiency, receipt of immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy within the preceding 12 months or long-term systemic corticosteroid therapy, receipt of immunoglobulin or any blood product transfusion within the last 3 months
* Female participants who are pregnant
* Any chronic illness that could, in the opinion of the Investigators, interfere with immune function or with the donation of large volumes of blood (e.g. thrombocytopaenia or coagulopathy, malabsorption disorders, chronic anaemia)
* An individual who is on the delegation log for the study
* Planned blood donation within 4 months of undergoing testing to assess whether the individual is a suitable Complement donor
18 Years
70 Years
ALL
Yes
Sponsors
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Wellcome Trust
OTHER
University of Oxford
OTHER
Responsible Party
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Principal Investigators
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Andrew Pollard, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Oxford
Locations
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Centre for Clinical Vaccinology and Tropical Medicine (CCVTM)
Oxford, Oxfordshire, United Kingdom
Countries
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Related Links
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Related Info
Other Identifiers
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2012/11
Identifier Type: -
Identifier Source: org_study_id
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