Phase
Condition
Lung Disease
Hiv
Treatment
N/AClinical Study ID
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adults aged 18-65 years
Resident in or near London or Oxford for the duration of the study period
Provide written informed consent
Willing to allow the investigators to review the volunteer's review NHS care record,medical history, blood results and radiographs.
Able and willing (in the investigator's opinion) to comply with all studyrequirements Group A and B Specific Inclusion Criteria
Have undergone screening for TB through NHS services (including IGRA testing +/- CXRwhere indicated)
Close contact with a sputum smear positive TB case within the last 12 weeks
Exclusion
Exclusion Criteria:
Participation in another research study involving receipt of an investigationalproduct in the 30 days preceding enrolment or during the trial follow up period.
History of anaphylaxis or any allergy likely to be exacerbated by any essentialstudy procedure
History of currently poorly controlled of airways disease (including asthma),current cancer (except BCC of the skin or CIS of the cervix), bleeding disorder, ordrug or alcohol abuse
Any significant autoimmune conditions or immunodeficiency (including HIV)
Previous diagnosis or treatment for TB disease or latent TB infection
Clinical, radiological, or laboratory evidence of current active TB disease
Previous receipt of any investigational TB vaccines or aerosolised BCG.
Clinically Significant abnormalities in spirometry.
Concurrent use of oral, inhaled or systemic steroid medication or use for more than 14 days within the last 6 months (steroids used as a cream or ointment arepermissible), or the use of other immunosuppressive agents concurrently or for morethan 14 days within the last 6 months
Use of antibiotics in the past 4 weeks.
Administration of immunoglobulins and/or any blood products within the three monthspreceding the planned study
Administration of a live vaccine within the preceding 28 days prior to enrolment.
Administration of any other non-live vaccine within the preceding 14 days prior toenrolment.
Pregnancy or intention to become pregnant during study period
Any other significant disease, disorder, or finding, which, in the opinion of theinvestigator, may either put the volunteer at risk, affect the volunteer's abilityto participate in the study or impair interpretation of the study data Group C Specific Exclusion Criteria
History of close contact with case of TB, or previous contact tracing by TBservices.
Study Design
Study Description
Connect with a study center
Churchill Hospital
Oxford, Oxfordshire OX3 7LE
United KingdomActive - Recruiting
Centre for Clinical Vaccinology and Tropical Medicine
Oxford, Oxon OX3 9DZ
United KingdomActive - Recruiting
Department of Respiratory Medicine, St Thomas' Hospital
London, SE1 7EH
United KingdomSite Not Available
Grove Building, Royal Free NHS Foundation Trust
London, NW3 2QG
United KingdomActive - Recruiting
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