Skip to content

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
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00125047
Enrollment
27231
Registered
2005-07-29
Start date
2001-10-31
Completion date
2007-08-31
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

Salmonellosis, 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 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.

Interventions

Single 0.5ml dose containing 25ug purified Vi polysaccharide of S. typhi.

BIOLOGICALHepatitis A vaccine

single 0.5ml dose contains 720 EL.U. of inactivated hepatitis A viral antigen

Sponsors

Aga Khan University
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 16 Years
Healthy volunteers
Yes

Inclusion criteria

* Registered in the project census * Age: 2-16 years

Exclusion criteria

* Fever \>37.5 degrees Celsius, axillary * Pregnancy * Lactating

Design outcomes

Primary

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

Secondary

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

Countries

Pakistan

Outcome results

None listed

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