Clinical Trials Directory

Trials / Completed

CompletedNCT00125047

Combined Vi Vaccination and Health Education Program on the Burden of Typhoid in Childhood

Effectiveness of a Combined Vi Vaccination and Health Education Program on Reducing the Burden of Typhoid During Childhood: A Demonstration Project in Karachi

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
27,231 (actual)
Sponsor
International Vaccine Institute · Academic / Other
Sex
All
Age
2 Years – 16 Years
Healthy volunteers
Accepted

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 Karachi, Pakistan. The cost-effectiveness of 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 due to the following reasons: 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. 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 3 urban slums in Pakistan. The vaccines used in this study are internationally produced and locally licensed. A complimentary, targeted, basic typhoid prevention health education program for the entire population at the initiation of the project will be provided and the actual Vi-demonstration project will be preceded by a 12-month typhoid surveillance activity. Secondary objectives of this trial are: * To monitor the adverse events following a routine Vi mass vaccination campaign; * To assess the knowledge, attitudes, beliefs and practices among parents and health care providers regarding typhoid illness, treatment and prevention; and * To study typhoid fever risk factors in the population. A nested, prospective matched case-control study is included in the trial in order to study typhoid risk factors among children in Karachi.

Conditions

Interventions

TypeNameDescription
BIOLOGICALTyphoid Vi vaccineSingle 0.5ml dose containing 25ug purified Vi polysaccharide of S. typhi.
BIOLOGICALHepatitis A vaccinesingle 0.5ml dose contains 720 EL.U. of inactivated hepatitis A viral antigen

Timeline

Start date
2001-10-01
Primary completion
2007-08-01
Completion
2007-08-01
First posted
2005-07-29
Last updated
2008-08-26

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT00125047. Inclusion in this directory is not an endorsement.