OPV as Potential Protection Against COVID-19

Sponsor
Bandim Health Project (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04445428
Collaborator
(none)
3,400
1
2
21.5
158

Study Details

Study Description

Brief Summary

Since the 1960s, studies have shown that oral polio vaccine (OPV) may have beneficial non-specific effects, reducing morbidity and mortality from other infections than polio. Such beneficial non-specific effect have been observed for other live vaccines, including measles, smallpox and BCG vaccine. For BCG, the vaccine for which the mechanism has been studied the most, the effects appear to be mediated through the innate immune system. The COVID-19 pandemic caused by the novel coronavirus SARS-CoV-2 has now caused over 7.1 million cases and

400,000 deaths worldwide. As everywhere else, it is anticipated that in Africa the older part of the population will be at risk of severe COVID-19. OPV is widely used in Africa, but for children. Both polio and coronavirus are positive-strand RNA viruses, therefore it is likely that they may induce and be affected by common innate immune mechanisms.

In a randomised trial at the Bandim Health Project in Guinea-Bissau, the investigators will assess the effect of providing OPV vs no vaccine to 3400 persons above 50 years of age. The trial will have the power to test the hypothesis that OPV reduces the combined risk of morbidity admission or death (composite outcome) by at least 28% over the subsequent 6 months.

Condition or Disease Intervention/Treatment Phase
  • Biological: oral polio vaccine + information
  • Behavioral: Information
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
3400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Care Provider, Outcomes Assessor)
Masking Description:
Participants are cluster randomised to OPV or no vaccine. Information on group assignment is not available to health center staff and staff at the health and demographic surveillance system
Primary Purpose:
Prevention
Official Title:
Oral Polio Vaccine as Potential Protection Against COVID-19: A Cluster-randomised Trial in Guinea-Bissau
Actual Study Start Date :
Jul 15, 2020
Actual Primary Completion Date :
Jan 31, 2022
Anticipated Study Completion Date :
May 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Standard dose bivalent oral polio vaccine, 0.1ml, and information regarding prevention of COVID-19

Biological: oral polio vaccine + information
Bivalent OPV (GSK), 0.1 ml administered orally on a sugar lump

Behavioral: Information
Advice regarding how to protect oneself from COVID-19

Other: Control

Information regarding prevention of COVID-19

Behavioral: Information
Advice regarding how to protect oneself from COVID-19

Outcome Measures

Primary Outcome Measures

  1. Mortality or infectious disease causing consultation or admission (Composite outcome) [6 months]

    Composite outcome of the first of death, hospitalisation for infection and/or consultation for infection at the health centre

Secondary Outcome Measures

  1. Self-reported morbidity [6 months]

    Episodes with self-reported infectious disease morbidity.

  2. Suspected COVID-19 infection [6 months]

    Episodes with self-reported infectious disease morbidity suspected to be caused by COVID (three or more of the following: fever, cough, sore thought, extreme fatigue, loss of smell/taste).

  3. Mortality [6 months]

    Either of the components of the composite outcome.

  4. Hospital admission for infectious disease [6 months]

    Either of the components of the composite outcome included repeated events.

  5. Consultations for infectious disease [6 months]

    Either of the components of the composite outcome included repeated events.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Living in a household which has had a census visit conducted after 1 January in 2017. Age above 50.
Exclusion Criteria:
  • Previous adverse events to OPV; Previous documented COVID-19; Acute severe infection.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bandim Health Project Bissau Guinea-Bissau

Sponsors and Collaborators

  • Bandim Health Project

Investigators

  • Principal Investigator: Ane Fisker, MD, PhD, Bandim Health Project

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Bandim Health Project
ClinicalTrials.gov Identifier:
NCT04445428
Other Study ID Numbers:
  • 77/CNES/INASA/2020
First Posted:
Jun 24, 2020
Last Update Posted:
Mar 18, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 18, 2022