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Evaluation of the Vi Polysaccharide Vaccine Against Typhoid Fever

Randomized Controlled Evaluation of the Vi Polysaccharide Vaccine Against Typhoid Fever in Eastern Kolkata, West Bengal, India

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00125008
Enrollment
37673
Registered
2005-07-29
Start date
2003-05-31
Completion date
2008-01-31
Last updated
2008-08-26

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

Conditions

Paratyphoid Fever, Typhoid

Keywords

Salmonella, Typhoid vaccine, enteric fever

Brief summary

This study is part of the International Vaccine Institute's (IVI's) typhoid Vi demonstration project that aims to accelerate the rational introduction of Vi vaccines in typhoid endemic countries. The purpose of this study is to determine the effectiveness of the Vi vaccine following a mass typhoid immunization campaign in an endemic area in Kolkata, India. The cost-effectiveness of the Vi vaccination and the logistic feasibility of a mass typhoid immunization campaign will also be evaluated.

Detailed description

Typhoid fever is a major cause of morbidity worldwide. The disease predominantly affects school-aged children, is more prevalent in urban areas, may last for several weeks and can lead to serious complications. Management of this disease is further complicated by the emergence of multi-drug resistant strains. Vaccination of high risk populations is considered the most promising strategy for the control of typhoid fever. The Vi polysaccharide vaccine has been targeted for accelerated introduction into public health programs since it has been shown to have consistent efficacy results even in areas of high typhoid incidence, is given as a single dose, lacks patent protection and requires less strict cold chain requirements. This project attempts to evaluate a new vaccination strategy for residents of endemic areas. A cluster-randomized trial involving the Vi polysaccharide vaccine and an active control (Hepatitis A) was designed to determine the effectiveness and the feasibility of providing Vi vaccine under actual programmatic conditions in 2 contiguous urban wards in Kolkata. The vaccines used in this study are internationally produced and locally licensed. A 1 year pilot phase will precede the actual Vi-demonstration project. Surveillance for typhoid fever cases will continue after the mass immunization campaign. A passive surveillance system to evaluate adverse events following immunization will be implemented. Socio-economic studies will be conducted in parallel to the effectiveness evaluation. The knowledge, attitudes, beliefs and practices among parents and health care providers regarding typhoid illness, treatment and prevention will be assessed. Logistic, feasibility and vaccine costs will also be determined.

Interventions

single 0.5ml dose (25ug of purified Vi polysaccharide of S. typhi)

BIOLOGICALHepatitis A vaccine

720 EL.U. of inactivated hepatitis A viral antigen for children 1440 EL.U. of inactivated hepatitis A viral antigen for adults

Sponsors

National Institute of Cholera and Enteric Diseases, India
CollaboratorOTHER
Wellcome Trust
CollaboratorOTHER
University of Western Ontario, Canada
CollaboratorOTHER
GlaxoSmithKline
CollaboratorINDUSTRY
International Vaccine Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
2 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Registered in the project census * Age \>=2 years * Provide informed consent to receive vaccine

Exclusion criteria

* Fever (\>37.5 degrees Celsius) * Pregnancy * Lactating

Design outcomes

Primary

MeasureTime frame
Total protection against S. typhi2 years from zero time

Secondary

MeasureTime frame
Indirect protection against S. typhi2 years from zero time
Overall protection against S. typhi2 years from zero time
Total protection against S. paratyphi2 years from zero time
Adverse event(s) following immunization30 days from vaccination

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026