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Clinical Trials/ISRCTN12131979
ISRCTN12131979
Completed
未知

Prospective, epidemiological, clinical and laboratory programme to plan and evaluate strategies to control enteric fever in different settings in Africa and Asia

niversity of Oxford0 sites423,618 target enrollmentOctober 20, 2016

Overview

Phase
未知
Intervention
Not specified
Conditions
Enteric fever
Sponsor
niversity of Oxford
Enrollment
423618
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

2017 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/28674145 protocol 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/34798028/ (added 03/02/2022)

Registry
who.int
Start Date
October 20, 2016
End Date
December 31, 2020
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Census study, WASH and HUS survey:
  • Census participants will be the population (n \=100,000, all ages) residing in a demarcated geographic area that is a known catchment population for each of the 3 typhoid surveillance sites. Participants will be recruited and consented as households.
  • 1\. Head of household / key informant is willing and competent to give informed consent for participation of the household in the study
  • 2\. Head of household / key informant is Male or Female, aged 18 years or above
  • 3\. Household is within the census area
  • Passive surveillance:
  • This component will include all patients presenting at any of the clinical surveillance sites in each country with a history of subjective fever \>72 hours with or without objective fever on presentation.
  • 1\. Individual willing and competent to give informed consent if \=18 years or the parent/legal guardian if participant \<18 years;
  • 2\. Able to comply with study requirements
  • 3\. In addition those considered index cases (for the household contact component) must be resident in a household enrolled in the census survey

Exclusion Criteria

  • Census study, WASH and HUS survey:
  • 1\. Head of household/key informant not willing for household to participate
  • 2\. Unable to identify Head of household/key informant
  • Passive surveillance:
  • 1\. Previous enrolment into this component (e.g. from previous attendance at healthcare facility with persistent fever)
  • 2\. Other underlying disease which can be rapidly diagnosed such as Malaria in children (Blantyre)
  • Household contacts (index cases):
  • 1\. Not a resident of household of index case at time of his/her primary illness
  • 2\. Fever at presentation in index case confirmed not due to S. Typhi or Paratyphi fever
  • 3\. Deemed clinically unsuitable by the survey team (e.g. terminally ill)

Outcomes

Primary Outcomes

Not specified

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