Clinical trial Recruiting at 1 site Observational

Assessing the impact of cholera vaccination in endemic areas

Official title: Cholera Control in Endemic Regions of Africa: Clinical Surveillance and Cholera Shedding Study in the Context of Mass Vaccination Campaigns, Democratic Republic of the Congo

Run by Epicentre · NCT04853186 · Data updated 2026-11-12

This study is testing if giving a cholera vaccine to lots of people in the Democratic Republic of the Congo can help keep cholera under control for at least two years.

More Cholera trials

Quick facts

Study typeObservational
SexAll
Enrollment6000 (estimated)
SponsorEpicentre
Academic / other
Locations1 site (Goma)
StatusRecruiting
StartedMay 11, 2021
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedSeptember 19, 2024
Trial IDNCT04853186 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals presenting at selected Cholera Treatment Centers who meet the case definition and provide consent.

Probably not a fit

Patients who decline to participate in the study will not benefit from the findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project evaluates the effectiveness of oral cholera vaccine mass campaigns in urban and rural areas of the Democratic Republic of the Congo (DRC). It includes clinical cholera surveillance to measure disease incidence, serological surveys to assess recent infection prevalence, and follow-up of individuals shedding V. cholerae. The goal is to determine if high vaccination coverage can sustain cholera control for at least two years. The findings will inform future cholera vaccination strategies in high-burden regions.

Why it matters

Potential benefit: If successful, this study could lead to improved cholera vaccination strategies, reducing incidence and mortality in endemic areas.

How similar studies have gone: Other studies have shown success with cholera vaccination campaigns, indicating potential for positive outcomes in similar approaches.

Who can join: the full rules

Show full inclusion / exclusion criteria
For Surveillance in study CTCs

Inclusion Criteria:

* All patients presenting at the time of the study to any selected Cholera Treatment Center/Cholera Treatment Unit (CTC/CTU), matching the case definition and giving his/her consent (or assent for children 8 to 17 years old) to participate in the study will be eligible.

Exclusion Criteria:

* Patients who decline to participate will be excluded from the study.

Follow up of individuals with active cholera shedding:

Inclusion Criteria:

1. present to any selected CTC/CTU, match the case definition, participate to the clinical surveillance activity and test positive to RDT OR
2. Be a household member of a person respecting inclusion criteria 1. AND for whom the head of the household has provided verbal consent to participate AND giving his/her consent (or assent for children 8 to 17 years old) to participate in the study will be eligible.

Exclusion Criteria:

\- Individuals who decline to participate will be excluded from the study, as well as households for whom the head of the household (and his or her representative) decline the participation of his/her household.

Where it's running

  • Anais Broban
    Goma, Democratic Republic of the Congo
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.