Enteric FeverNCT03554213
Typhoid Conjugate Vaccine Introduction in Navi Mumbai, India
An observational study of Enteric Fever and Typhoid Fever, run by Stanford University at 6 sites in India.
Trial summary
The purpose of this study is to evaluate the impact of a government-led typhoid conjugate vaccine introduction program on typhoid disease burden in Navi Mumbai, India. Read more about this study
- Who is it for?
- Ages 6 months to 16 yearsHealthy volunteers can take part
- Conditions the study is for
- Enteric Fever, Typhoid Fever, Salmonella Typhi Infection
- What is being tested?
- Typhoid Conjugate Vaccine
- Type of treatment
- Vaccines
- How many people
- 17,292 participants
- Where
- 6 sitesIndia
- Study dates
- 2 Jul 2018to 31 Mar 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 6 months to 16 years
- All sexes
- Healthy volunteers accepted
- Child
Study population: The focus of this study is children age 6 months to 16 years living in areas governed by Navi Mumbai Municipal Corporation (NMMC). The age range of children eligible to receive typhoid conjugate vaccine (TCV) in NMMC's TCV introduction program is 9 months to 15 years. For community surveys, only households with children <16 years old will be selected. The evaluation study will examine a slightly broader age range than NMMC's TCV vaccination program because TCV is licensed for >6 month old children and because the vaccine introduction will occur over 1 year thus the oldest eligible children will be 16 years old at study end.
Who may be able to join
- For overall study,
- For hospital-based surveillance, children age 6 months to 16 years.
- For community-based surveys, adult members of households with children <16 years old.
- Parental consent (and child assent for >12 years) given.
- For hospital-based surveillance for typhoid fever, additional criteria include: history of fever for >72 hours within the last 7 days without upper respiratory tract symptoms and vesicular rash; strong clinical suspicion of enteric fever including ileal perforations; or diagnosis of enteric fever confirmed by positive blood cultures or histopathology. For outpatients, additional criterion of living in areas governed by Navi Mumbai Municipal Corporation.
- For hospital-based surveillance of adverse events of special interest, timing will focus on one month prior to and 42 days after the vaccination campaign. Diagnoses included are: anaphylaxis, bronchospasm, urticaria, Guillain-Barré syndrome, meningitis, encephalitis, myelitis, seizures, thrombocytopenia, and sudden death.
- For all community surveys, additional criterion of living in areas governed by Navi Mumbai Municipal Corporation.
Who cannot join
- For all study components,
- Already enrolled in same study component.
- No informed consent or assent given.
- For hospital-based surveillance for typhoid fever, additional exclusion criteria are: fever <72 hours, symptoms of upper respiratory tract infection (coryza, rhinorrhea), and vesicular exanthem. For outpatients, those living outside of NMMC-governed areas will be excluded.
- For community surveys, households without children <16 years old and households in which there is no adult (>18 years old) at time of survey will be excluded.
Trial locations and contacts
6 sites in 1 country.
6 sites in 1 country
India6 sites
D. Y. Patil Medical College and Hospital, Nerul
Navi Mumbai
Dr. Joshi's Central Clinical Microbiology Laboratory, Vashi
Navi Mumbai
Dr. Yewale Multispecialty Hospital for Children, Vashi
Navi Mumbai
Mahatma Gandhi Memorial (MGM) New Bombay Hospital, Vashi
Navi Mumbai
Mathadi Hospital Trust, Koparkharaine
Navi Mumbai
Navi Mumbai Municipal Corporation (NMMC) General Hospital, First Referral Unit (FRU), Vashi
Navi Mumbai
About this study
Official title: Evaluation of a Typhoid Conjugate Vaccine Introduction Program in Navi Mumbai, India
The purpose of this study is to evaluate the impact of a government-led typhoid conjugate vaccine introduction program on typhoid disease burden in Navi Mumbai, India.
Read the detailed description
A new generation of typhoid conjugate vaccines (TCVs) have been shown to be safe and provide long-lasting immunity in children. In India, Typbar TCV Vi-TT (Vi capsular polysaccharide conjugated with tetanus toxoid protein) is manufactured by Bharat Biotech International Limited (BBIL). Immunogenicity studies by BBIL showed >90% detectable antibodies to Typbar TCV vaccine at 42 days and >70% at 720 days in persons 2-45 years old. A single dose of vaccine was effective in children 6-23 months old with 98% seroconversion at 42 days and persistent high antibody titers at 720 days. Another randomized controlled trial study by University of Oxford tested Vi-TT with a human challenge model of typhoid fever in which participants ingested Salmonella Typhi after vaccination. Typhoid fever was diagnosed by clinical criteria and/or positive blood culture at 2 weeks in 77% of controls (n=31) as compared to 35% in the Vi-TT group (n=37) to give vaccine efficacy of 54% (95% confidence interval of 26-71). Typbar TCV has been licensed in India for children >6 months old since 2013 and is currently used in the private sector. In January 2018, the World Health Organization (WHO) recommended the use of typhoid conjugate vaccines especially in those countries with the highest burden of disease and the highest burden of antimicrobial resistance. However, there are no field effectiveness studies yet for Typbar TCV.
In this study, a hybrid facility- and community-based typhoid surveillance strategy will be used to evaluate the impact of a government-led typhoid conjugate vaccine introduction program on typhoid disease burden in Navi Mumbai, India. Navi Mumbai is a metropolitan area extending from Mumbai with approximately 1.4 million people and wide demographic and socioeconomic strata, including slums. Navi Mumbai is comprised of 13 area nodes, and 8 of these nodes are under the jurisdiction of the local government body, Navi Mumbai Municipal Corporation (NMMC). Navi Mumbai has high enteric fever burden: a 2008 study found 98 blood culture-confirmed pediatric cases over 16 months in 2 hospitals with a majority of isolates exhibiting multi-drug resistance. Data from one private laboratory in 2015 showed over 225 S. Typhi cases including 3 cases with ceftriaxone resistance.
NMMC has decided to introduce TCV into public sector routine immunization services and will vaccinate all children 9 months to <15 years old within its jurisdiction - estimated 390,000 children - with TCV over 2 years. NMMC government officials are collaborating with researchers from WHO India, Institute of Cholera and Enteric Diseases (NICED), Centers for Disease Control and Prevention (CDC), and Stanford University to implement the TCV introduction in a two-phase cluster-randomized program in order to allow rigorous evaluation of population impact. NMMC has 22 urban health posts (UHPs) that give routine childhood immunizations. UHPs were first grouped into 3 strata based on % of population living in slums: low, medium, or high. Half of the UHPs within each stratum were then randomly selected to receive TCV in 2018 (Phase 1) and the remaining UHPs to receive TCV one year later in 2019 (Phase 2).
Evaluation studies of NMMC's TCV introduction program include: impact on blood-culture confirmed typhoid fever; impact on clinical syndromes of febrile illness; vaccine safety; vaccine efficacy; vaccination campaign coverage and acceptability surveys; environmental water contamination with Salmonella Typhi; seroconversion associated with typhoid infection; and cost-effectiveness of typhoid conjugate vaccination campaign.
- Conditions
- Enteric Fever, Typhoid Fever, Salmonella Typhi Infection
- Being tested
- Typhoid Conjugate Vaccine
- Medical subject headings
- Typhoid Fever
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Typhoid Conjugate VaccineBiological
Typbar TCV Vi-TT (Vi capsular polysaccharide conjugated with tetanus toxoid protein) manufactured by Bharat Biotech International Limited
| Study group | Role | What they receive |
|---|---|---|
| Phase 1: TCV in 2018 | Children receiving TCV (typhoid conjugate vaccine) in 2018 vaccination campaign by NMMC. Receives: Biological: Typhoid Conjugate Vaccine | |
| Phase 2: TCV in 2019 | Children receiving TCV (typhoid conjugate vaccine) in 2019 vaccination campaign by NMMC. Receives: Biological: Typhoid Conjugate Vaccine |
What is being measured
The primary outcome is the main question the study is designed to answer.
blood culture-confirmed typhoid fever
Hospital surveillance for typhoid fever diagnosed by blood cultures will be conducted at 6 study sites in Navi Mumbai: 5 hospitals and 1 independent laboratory.
Measured: up to 24 months
Secondary outcomes (6)
Adverse events following immunization
Evaluation of safety and adverse events following immunization (AEFI) during Phase I of TCV introduction in 2018. Three safety evaluations include: 1) routine national AEFI surveillance system reports, 2) active follow-up by phone of a subset of vaccine recipients at 48hrs and 7 days post vaccination, and 3) hospital-based surveillance at 5 hospital study sites conducting typhoid fever surveillance examining patient records for adverse events of special interest in both vaccinated and unvaccinated populations
Measured: up to 4 months
vaccination coverage
Community surveys estimating TCV coverage achieved by the vaccination campaign in the public sector during phase 1 (and potentially phase 2 if funding allows) as well as vaccine acceptability, refusals, knowledge, attitudes, and social mobilization strategies.
Measured: up to 18 months
environmental water contamination with Salmonella Typhi
Molecular testing of household and municipal water samples for presence of Salmonella Typhi and Paratyphi A and impact of TCV vaccination program on water contamination.
Measured: up to 24 months
seroconversion associated with typhoid infection
Collect dried blood spots in subset of household surveys and store for future testing of antibodies associated with typhoid infection (once other research studies on best antibody tests have resulted).
Measured: up to 24 months
cost-effectiveness of typhoid conjugate vaccination campaign
Plan to develop a tool and to estimate the delivery cost of TCV, to estimate the cost of illness (COI) related to typhoid fever, and ultimately to estimate the cost-effectiveness of typhoid conjugate vaccination campaign conducted in Navi Mumbai.
Measured: up to 24 months
clinical syndromes of febrile illness
Community-based surveys of clinical syndromes of febrile illness and healthcare utilization in NMMC-governed areas (same as TCV vaccination areas).
Measured: up to 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Jun 2018
- Study start2 Jul 2018
- Primary completion31 Mar 2021
- Study completion31 Mar 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Enteric FeverStudies of the same condition, open and under way.
- More trials run by Stanford UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 17,292 participants (actual)
Sponsor and investigators
- Lead sponsor
- Stanford University
- Sponsor type
- University, hospital or other
- Collaborators
- Centers for Disease Control and Prevention, World Health Organization, National Institute of Cholera and Enteric Diseases, India, Bill and Melinda Gates Foundation
- Responsible party
- Principal investigator, Stephen P Luby, Stanford University
- Investigators
- Stephen Luby, MD, Principal investigator, Stanford UniversityKashmira Date, MD MPH, Principal investigator, Centers for Disease Control and PreventionShanta Dutta, MD PhD, Principal investigator, National Institute of Cholera and Enteric Diseases (NICED)Pankaj Bhatnagar, MD, Principal investigator, World Health Organization (WHO) - India
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03554213
- Sponsor's protocol ID
- IRB-39627
- Other IDs
- OPP1169264
- Status last verified
- Sep 2021
- First submitted
- 30 May 2018
- Last updated
- 4 Oct 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Oct 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of a Typhoid Conjugate Vaccine Introduction Program in Navi Mumbai, India
- ClinicalTrials.gov ID
- NCT03554213
- Acronym / sponsor ID
- IRB-39627
- Conditions
- Enteric Fever, Typhoid Fever, Salmonella Typhi Infection
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 17,292 participants (actual)
- Lead sponsor
- Stanford UniversityUniversity, hospital or other
- Collaborators
- Centers for Disease Control and Prevention, World Health Organization, National Institute of Cholera and Enteric Diseases, India, Bill and Melinda Gates Foundation
- Study start
- 2 Jul 2018 (actual)
- Primary completion
- 31 Mar 2021 (actual)
- Study completion
- 31 Mar 2021 (actual)
- First posted
- 13 Jun 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to evaluate the impact of a government-led typhoid conjugate vaccine introduction program on typhoid disease burden in Navi Mumbai, India.
Detailed description
A new generation of typhoid conjugate vaccines (TCVs) have been shown to be safe and provide long-lasting immunity in children. In India, Typbar TCV Vi-TT (Vi capsular polysaccharide conjugated with tetanus toxoid protein) is manufactured by Bharat Biotech International Limited (BBIL). Immunogenicity studies by BBIL showed >90% detectable antibodies to Typbar TCV vaccine at 42 days and >70% at 720 days in persons 2-45 years old. A single dose of vaccine was effective in children 6-23 months old with 98% seroconversion at 42 days and persistent high antibody titers at 720 days. Another randomized controlled trial study by University of Oxford tested Vi-TT with a human challenge model of typhoid fever in which participants ingested Salmonella Typhi after vaccination. Typhoid fever was diagnosed by clinical criteria and/or positive blood culture at 2 weeks in 77% of controls (n=31) as compared to 35% in the Vi-TT group (n=37) to give vaccine efficacy of 54% (95% confidence interval of 26-71). Typbar TCV has been licensed in India for children >6 months old since 2013 and is currently used in the private sector. In January 2018, the World Health Organization (WHO) recommended the use of typhoid conjugate vaccines especially in those countries with the highest burden of disease and the highest burden of antimicrobial resistance. However, there are no field effectiveness studies yet for Typbar TCV.
In this study, a hybrid facility- and community-based typhoid surveillance strategy will be used to evaluate the impact of a government-led typhoid conjugate vaccine introduction program on typhoid disease burden in Navi Mumbai, India. Navi Mumbai is a metropolitan area extending from Mumbai with approximately 1.4 million people and wide demographic and socioeconomic strata, including slums. Navi Mumbai is comprised of 13 area nodes, and 8 of these nodes are under the jurisdiction of the local government body, Navi Mumbai Municipal Corporation (NMMC). Navi Mumbai has high enteric fever burden: a 2008 study found 98 blood culture-confirmed pediatric cases over 16 months in 2 hospitals with a majority of isolates exhibiting multi-drug resistance. Data from one private laboratory in 2015 showed over 225 S. Typhi cases including 3 cases with ceftriaxone resistance.
NMMC has decided to introduce TCV into public sector routine immunization services and will vaccinate all children 9 months to <15 years old within its jurisdiction - estimated 390,000 children - with TCV over 2 years. NMMC government officials are collaborating with researchers from WHO India, Institute of Cholera and Enteric Diseases (NICED), Centers for Disease Control and Prevention (CDC), and Stanford University to implement the TCV introduction in a two-phase cluster-randomized program in order to allow rigorous evaluation of population impact. NMMC has 22 urban health posts (UHPs) that give routine childhood immunizations. UHPs were first grouped into 3 strata based on % of population living in slums: low, medium, or high. Half of the UHPs within each stratum were then randomly selected to receive TCV in 2018 (Phase 1) and the remaining UHPs to receive TCV one year later in 2019 (Phase 2).
Evaluation studies of NMMC's TCV introduction program include: impact on blood-culture confirmed typhoid fever; impact on clinical syndromes of febrile illness; vaccine safety; vaccine efficacy; vaccination campaign coverage and acceptability surveys; environmental water contamination with Salmonella Typhi; seroconversion associated with typhoid infection; and cost-effectiveness of typhoid conjugate vaccination campaign.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Phase 1: TCV in 2018 | – | Biological: Typhoid Conjugate VaccineChildren receiving TCV (typhoid conjugate vaccine) in 2018 vaccination campaign by NMMC. |
| Phase 2: TCV in 2019 | – | Biological: Typhoid Conjugate VaccineChildren receiving TCV (typhoid conjugate vaccine) in 2019 vaccination campaign by NMMC. |
Who may qualify
- Ages
- 6 months to 16 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
- Study population
- The focus of this study is children age 6 months to 16 years living in areas governed by Navi Mumbai Municipal Corporation (NMMC). The age range of children eligible to receive typhoid conjugate vaccine (TCV) in NMMC's TCV introduction program is 9 months to 15 years. For community surveys, only households with children <16 years old will be selected. The evaluation study will examine a slightly broader age range than NMMC's TCV vaccination program because TCV is licensed for >6 month old children and because the vaccine introduction will occur over 1 year thus the oldest eligible children will be 16 years old at study end.
Key inclusion criteria (7 listed)
- For overall study,
- For hospital-based surveillance, children age 6 months to 16 years.
- For community-based surveys, adult members of households with children <16 years old.
- Parental consent (and child assent for >12 years) given.
- For hospital-based surveillance for typhoid fever, additional criteria include: history of fever for >72 hours within the last 7 days without upper respiratory tract symptoms and vesicular rash; strong clinical suspicion of enteric fever including ileal perforations; or diagnosis of enteric fever confirmed by positive blood cultures or histopathology. For outpatients, additional criterion of living in areas governed by Navi Mumbai Municipal Corporation.
Key exclusion criteria (5 listed)
- For all study components,
- Already enrolled in same study component.
- No informed consent or assent given.
- For hospital-based surveillance for typhoid fever, additional exclusion criteria are: fever <72 hours, symptoms of upper respiratory tract infection (coryza, rhinorrhea), and vesicular exanthem. For outpatients, those living outside of NMMC-governed areas will be excluded.
- For community surveys, households without children <16 years old and households in which there is no adult (>18 years old) at time of survey will be excluded.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Typhoid Conjugate VaccineTypbar TCV Vi-TT (Vi capsular polysaccharide conjugated with tetanus toxoid protein) manufactured by Bharat Biotech International Limited | Biological | Phase 1: TCV in 2018, Phase 2: TCV in 2019 |
Primary outcome
blood culture-confirmed typhoid fever
Time frame: up to 24 months
Hospital surveillance for typhoid fever diagnosed by blood cultures will be conducted at 6 study sites in Navi Mumbai: 5 hospitals and 1 independent laboratory.
6 secondary outcomes
Adverse events following immunization
Time frame: up to 4 months
vaccination coverage
Time frame: up to 18 months
environmental water contamination with Salmonella Typhi
Time frame: up to 24 months
seroconversion associated with typhoid infection
Time frame: up to 24 months
cost-effectiveness of typhoid conjugate vaccination campaign
Time frame: up to 24 months
clinical syndromes of febrile illness
Time frame: up to 18 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Oct 2021.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Stephen Luby, MD principal investigator
Stanford University
Kashmira Date, MD MPH principal investigator
Centers for Disease Control and Prevention
Shanta Dutta, MD PhD principal investigator
National Institute of Cholera and Enteric Diseases (NICED)
6 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Enteric Fever and Typhoid Fever, run by Stanford University at 6 sites in India.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Oct 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 6 sites in India. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
blood culture-confirmed typhoid fever (time frame: up to 24 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Oct 2021.