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CompletedNCT04423159CHOVAXIMUpdated Jul 20, 2022

Immunological Characteristics of a Population at Risk of Cholera After Oral Cholera Vaccine (CHOVAXIM)

An interventional study of OCV Vaccine in Diarrhea Infectious, sponsored by Centre for Infectious Disease Research in Zambia. Completed at 1 site in Zambia. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-07-20.

Sponsored by Centre for Infectious Disease Research in Zambia · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
225
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The purpose of the study is to find out if individuals who received first and second dose of Oral Cholera Vaccine (OCV) in Lukanga Swamps, Central Province of Zambia have developed protection against future attacks to cholera. The investigators also want to investigate whether vitamin A deficiency and being HIV positive increases the chances of suffering from cholera.

Read the detailed description

Cholera is caused by toxigenic strains of Vibrio cholerae O1 and O139 and is characterised by sudden onset of acute watery diarrhoea that can lead to severe dehydration and ultimately death if not treated. Zambia, has continued to experience cholera outbreaks in several parts of the country. In order to curb the disease outbreaks, the World Health Organisation (WHO) recommended introducing cholera vaccination as a supplementary cholera control measure together with other prevention and control strategies, in endemic areas as well as in other places at risk for cholera outbreaks. OCV has recently been introduced to Zambia where a large population was vaccinated with 1 dose of Shanchol®, and about 6 months later over 70% individuals traced to receive a second dose.

Considering the annual outbreaks of cholera in Zambia, there is urgent need to determine whether Shanchol® is able to elicit a sufficient and specific immunological response in individuals who received OCV in Zambia. This study will also help the investigator understand whether there are immune response differences based on genetics and may indicate whether some people may need more vaccine regimens than others.

Objective 1: To profile cholera specific antibody status of a population at risk of cholera before and after receiving 1st and 2nd dose of shanchol ® oral cholera vaccine (OCV) Objective 2: To profile and characterize cholera specific B and T lymphocyte phenotypes among the immunized Zambians Objective 3: Develop and evaluate a non-invasive proxy measure of OCV immune responses Objective 4: To measure the protective value of immunizing HIV-infected individuals through measurement of the neutralization capabilities OCV generated antibodies Objective 5: To assess the impact of ABO blood groups on cholera antibody generation

02

Conditions studied

  • Diarrhea Infectious

Keywords

  • Diarrhea
  • HIV
  • Vaccines
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Participants aged 18-65 years are eligible to participate.
  • Participant is a resident of the study area. Residence was defined as individuals living in the study area for the past 1 year.
  • Written consent provided by participant.

Exclusion criteria

Exclusion Criteria:

  • Participant aged less than 18 years
  • Refuses to consent to participate
  • Pregnancy
  • Participant has acute medical illness prior to receipt of oral cholera vaccine -Participant has a history of hospitalization for cholera in the past one week
04

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
225 participants (actual)

Study arms

  • Experimental
    OCV vaccine

    Shanchol 1.5mL to be administered orally. Each dose contains V.cholerae O1 Inaba El Tor Strain, Inaba classical strain, ogawa classical strain and O139 strain. As well as Thiomersal and a buffer

    Biological: OCV Vaccine

Interventions

  • BiologicalOCV Vaccine

    2 doses of OCV were administered to all enrolled participants 1st dose administered at baseline and second dose administered 28 days post 1st dose.

05

What researchers measure

Primary outcomes

  1. Vibriocidal

    The primary aim of this project is to determine changes in the vibriocidal geometric mean titers at 6, 12, 24, 30, 36, 42 and 48 months (GMT) in participants who receive the second dose of oral cholera vaccine (OCV) at 28 days .

    Time frame: 4 years

Secondary outcomes

  1. Vibriocidal

    Vibriocidal Antibody Response Rates in HIV infected individuals

    Time frame: 4 years

  2. Vibriocidal

    Detection of vibriocidal antibodies in saliva and compare to serum at 1 year post OCV vaccination

    Time frame: 1 year

06

Study locations

1 site
  • Waya clinic
    Kabwe, Central 10101, Zambia
07

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT04423159
Lead sponsor
Centre for Infectious Disease Research in Zambia
Collaborators
Johns Hopkins University, European and Developing Countries Clinical Trials Partnership (EDCTP)
Responsible party
Sponsor
First posted
Jun 9, 2020
Start date
Oct 16, 2016
Primary completion
Oct 31, 2020
Completion
Oct 31, 2020
Last update
Jul 20, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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