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BCG vaccination against COVID-19

Not Applicable
Registration Number
CTRI/2020/06/025854
Lead Sponsor
Indian Council of Medical Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Elderly individuals 60 years â?? 95 years of age with general good health, as confirmed by history and physical examination.

2) No known history of HIV or on immunosuppressive drugs for malignancy or transplant

3) Provide a signed and dated informed consent form

Elderly individuals with or without co-morbid conditions like Diabetes mellitus, or Hypertension or Hyperlipidemia will be considered for this study, if they are on regular treatment.

Exclusion Criteria

1) Positive for SARS-Cov2 infection, by either antibody (serology) or PCR test

2) Known HIV or malignancy or Transplant recipient or on Dialysis

3) Individuals on immune-suppressive therapies or treatments for malignancy or transplant / dialysis / anti-retroviral treatment

4) Recently (in the last 6-months) diagnosed with TB or currently on anti-TB treatment or anti-psychiatric medications

5) Has any BCG vaccine contraindication like allergy or hypersensitivity to BCG, individuals with HIV infection, leukaemia, malignant lymphoma, chronic granulomatous disease,

6) H/o of previous administration of experimental MTB vaccines within the past 6 months.

7) Sick and moribund individuals with Karnofsky score <50

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion of patients with Severe COVID disease based on COVID Severity Scale and proportion of death due to Covid 19 disease <br/ ><br>Timepoint: 6 months post vaccination
Secondary Outcome Measures
NameTimeMethod
1. Proportion of Hospital admission and ICU admission due to Covid-19 <br/ ><br>2. Proportion of participants in various Severity stages of Covid-19 (mild, moderate or severe) <br/ ><br>3. Proportion of participants requiring hospital admission due to other respiratory febrile illness <br/ ><br>4. Immunological outcomes in the sub study <br/ ><br>Timepoint: At 6 months post vaccination
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