Status:
ACTIVE_NOT_RECRUITING
Long Term Effects of BCG Vaccination on Infectious and Immune Mediated Diseases
Lead Sponsor:
Radboud University Medical Center
Collaborating Sponsors:
UMC Utrecht
Conditions:
BCG Vaccination Reaction
Infections
Eligibility:
All Genders
60+ years
Brief Summary
Rationale: The effects of BCG vaccination have been only sporadically studied in the elderly, and the long-term effects of the vaccination have not been studied until now. There is evidence that BCG v...
Eligibility Criteria
Inclusion
- Completed participation in the BCG-CORONA-ELDERLY or BCG-PRIME study
- Given consent to be approached for further studies
Exclusion
- Has received a BCG vaccination after the BCG-CORONA-ELDERLY or BCG-PRIME study
- Inclusion Criteria from BCG-PRIME:
- Age ≥60 years
- Meeting at least one of the following criteria:
- Having a chronic somatic disease\*
- Having undergone major surgery\*\*
- Planned to be discharged from the hospital or discharged from the hospital less than 6 weeks ago; a hospital admission is defined as an overnight stay. Departments of interest are those that in the opinion of the principle investigator admit mostly vulnerable elderly and include but are not limited to: cardiology, pulmonology, internal medicine, neurology.
- Attending the thrombosis care service \* Chronic somatic diseases do not include risk factors such as hypertension or obesity unless the participant receives medication targeted against the risk factor.
- Major surgery is any invasive operative procedure in which a more extensive resection is performed, e.g. a body cavity is entered, organs are removed, or normal anatomy is altered. In general, if a mesenchymal barrier is opened (pleural cavity, peritoneum, meninges), the surgery is considered major
- Exclusion criteria from BCG-PRIME:
- Fever (\>38 ºC) within the past 24 hours
- Suspicion of current active viral or bacterial infection; the requirement to finish an antibiotic course upon discharge is not an exclusion criterion when the infection is controlled in the opinion of the attending physician
- Vaccination with live vaccine in the past four weeks or planned vaccination with live vaccine during the next four weeks
- Severely immunocompromised participants. This exclusion category comprises:
- known infection by the human immunodeficiency virus (HIV-1);
- neutropenic with less than 500 neutrophils/mm3;
- solid organ transplantation;
- bone marrow transplantation;
- hematological malignancy;
- chemo-, radio- or immunotherapy for solid organ malignancy in the past 6 months;
- primary immunodeficiency;
- severe lymphopenia with less than 400 lymphocytes/mm3;
- treatment with any immunosuppressant drugs such as anti-cytokine therapies, and treatment with oral or intravenous steroids defined as daily doses of \>10 mg/day or a cumulative dose of \>700 mg prednisone or equivalent for other corticosteroids in the three months prior to enrolment, or probable use of oral or intravenous steroids in the following four weeks;
- receiving chronic renal replacement therapy.
- Known history of a positive Mantoux or active TB; prior BCG vaccination or a positive Mantoux test after BCG vaccination without confirmation of TB are NOT an exclusion criterion.
- Born in a country with high incidence of TB (see supplement B)
- Active participation in another research study that involves BCG administration
- History of documented COVID-19 (self-reported by the participant: either confirmed by a microbiological test or with clinical diagnosis during hospitalization)
- Not able to perform the study procedures as judged by the attending physician
- Legally incapacitated or unwilling to provide informed consent
- Inclusion criteria from BCG-CORONA-ELDERLY:
- Adult (≥ 60 years)
- Written informed consent
- Exclusion criteria from BCG-CORONA-ELDERLY:
- Fever (\>38 ºC) within the past 24 hours
- Suspicion of current active viral or bacterial infection
- Expected vaccination during the first three months of the study period
- Severely immunocompromised subjects. This exclusion category comprises: a) subjects with known infection by the human immunodeficiency virus (HIV-1); b) neutropenic subjects with less than 500 neutrophils/mm3; c) subjects with solid organ transplantation; d) subjects with bone marrow transplantation; e) subjects under chemotherapy; f) subjects with primary immunodeficiency; g) severe lymphopenia with less than 400 lymphocytes/mm3; h) treatment with any immunosuppressant drugs such as anti-cytokine therapies, and treatment with oral or intravenous steroids defined as daily doses of 10mg prednisone or equivalent for longer than 3 months, or probable use of oral or intravenous steroids in the following four weeks
- Active solid or non-solid malignancy or lymphoma within the prior two years
- Active participation in another research study that involves BCG administration
Key Trial Info
Start Date :
May 20 2022
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 20 2027
Estimated Enrollment :
4292 Patients enrolled
Trial Details
Trial ID
NCT05387655
Start Date
May 20 2022
End Date
June 20 2027
Last Update
April 20 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Radboud university medical center
Nijmegen, Gelderland, Netherlands, 6525GA