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Effectiveness of a Bivalent Killed Whole Cell Based Oral Cholera Vaccine

Effectiveness of a Bivalent, Killed Whole-cell Based Oral Cholera Vaccine(Shanchol®) Delivered Through Community-based Mass Vaccination Campaign in a High-risk Population in India: Matched Case-control Studies

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01508507
Enrollment
240
Registered
2012-01-12
Start date
2013-03-31
Completion date
2014-03-31
Last updated
2013-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholera

Keywords

Oral, Cholera, Vaccine, Herd, Risk, population, Matched, Control, Case, Bias

Brief summary

Various field studies has found that the modified , bivalent, whole cell - based oral cholera vaccine (OCV) to be safe, immunogenic and effective with protective efficacy of 67 % in earlier clinical trials. However, the effectiveness of the vaccine in real life situation using the public health system is unknown. It is critical to follow up in the same population, where pilot introduction of OCV was introduced and evaluate vaccine proactive effectiveness at individual as well as at population level. The follow - up and determination of effectiveness of mass OCV vaccination was requested by State Government.

Detailed description

The overall goal of this study is to evaluate the protective effectiveness of one or two doses of modified, bivalent, killed whole cell based OCV, given at least 14 days apart, when delivered through community - based mass vaccination campaign using existing public health infrastructure in a high - risk population in Satyabadi block of Puri district, Orissa, India. This study has following objectives Primary objectives: \* To evaluate the individual level protective effectiveness of one or two doses of OCV against culture confirmed cholera episodes, severe enough to seek a formal health care. Secondary objectives: * To evaluate population - level effectiveness (herd effects)of OCV delivered through a community based mass vaccination when the vaccine is delivered to more than half of population at risk. * To determine inverse correlation between vaccine coverage and cholera incidence among diverse geographical clusters.

Interventions

None listed

Sponsors

Department of Health and Family Welfare, Orissa
CollaboratorOTHER
Regional Medical Research Center, Orissa
CollaboratorUNKNOWN
International Vaccine Institute
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to No maximum
Healthy volunteers
No

Inclusion criteria

for cases of the main case-control study are as follows: * Giving verbal informed consent/assent, or in the case of minors, a parent or guardian give informed consent to participate in the study * Living in the study area since the start of the mass vaccination * Submitted a faecal specimen * Whose residence could be located * Whose stool specimens yield V. cholera O1 or O139 * Belonging to study population through census database

Exclusion criteria

* Not giving verbal informed consent/assent, or in the case of minors, a parent or guardian does not give informed consent to participate in the study * Not living in the study area since the start of the mass vaccination * No faecal specimen * Whose residence could not be located * Whose stool specimens does not yield V. cholera O1 or O139 * Not belonging to study population through census database

Design outcomes

Primary

MeasureTime frameDescription
Vaccine protective effectiveness at individual level11 monthsMatched controls will be selected among the persons of the same age group as that of each case. 1 to 4 ratio will be used in matching cases to controls.Information on all other exposure variables will be collected through questionaire interview for both cases and controls.Protective effectiveness (PE) (%) = \[1- the odds of vaccination among cholera confirmed cases relative to the odds of vaccination among matched controls\] × 100 is the metric to measure vaccine protective effectiveness at individual level.

Secondary

MeasureTime frameDescription
Population level effectiveness (herd effect)11 monthsIndirect effect: Fraction of household members who are vaccinated in households of unvaccinated cases compared with fraction of household members who are vaccinated in households of unvaccinated controls Total effect: Fraction of household members who are vaccinated in households of vaccinated cases compared with the fraction of household members who are vaccinated in households of vaccinated controls. Overall effects: Fraction of household members who are vaccinated in household of cases compared with fraction of household members who are vaccinated in control households.
Cohort / GIS study for the measure of herd protection11 monthsGeographic unit as a cluster for evaluating vaccine herd protection with the use of cohort analysis, using GIS information from the baseline census. Here, there will be comparison in the incidence of the target outcome (cholera or non-cholera diarrhea) according to the level of vaccine coverage of the geographic unit.

Countries

India

Contacts

Primary ContactVijaya Laxmi Mogasale, MBBS, MD, DPH (Nut)
VijayaLaxmi.Mogasale@ivi.int+822 - 8811 442
Backup ContactAnuj Bhattachan, MBBS, MPH
abhattachan@ivi.int+822 - 8811 255

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026