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Surveillance of Hospitalised Pneumonia and Bacterial Meningitis in Tône District, Togo, 2010-2013

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01747369
Enrollment
2000
Registered
2012-12-11
Start date
2010-04-30
Completion date
2017-06-30
Last updated
2017-03-06

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

Conditions

Meningitis, Bacterial, Pneumonia, Bacterial, Pneumonia, Viral

Keywords

surveillance study, prospective, observational, health center-based, pneumonia, bacterial, pneumonia, viral, meningitis, bacterial, Africa south of the Sahara

Brief summary

The aim of this study is to estimate the burden of disease due to pneumococci, other bacteria and viruses in the African meningitis belt prior to pneumococcal conjugate vaccine introduction and to estimate the population impact of the vaccine after its implementation in 2014. In a defined population of a sanitary district in northern Togo, during the period 2010 to 2017, investigators enroll patients of all ages with suspected pneumonia requiring hospitalization or suspected bacterial meningitis. Patients are evaluated by bacteriology and molecular biology techniques on blood, cerebro-spinal fluid, nasal aspirates and by chest X-ray.

Interventions

None listed

Sponsors

Region Sanitaire des Savanes, Togo
CollaboratorUNKNOWN
Ministere de la Sante et de la Promotion Sociale, Togo
CollaboratorUNKNOWN
Institut National d'Hygiene, Togo
CollaboratorUNKNOWN
Centre Muraz
CollaboratorOTHER
Fondation Mérieux, France
CollaboratorUNKNOWN
Pfizer
CollaboratorINDUSTRY
Agence de Médecine Préventive, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Pneumonia surveillance: Inclusion Criteria: * resident of Tône sanitary district - requiring hospitalisation for at least one night for clinical pneumonia syndrome * hospitalised in a study site during the study period

Exclusion criteria

* absence of informed consent by patient or legal tutor Meningitis surveillance: Inclusion Criteria: * resident of Tône sanitary district * presenting clinical signs of acute bacterial meningitis * hospitalised in a study site during the study period

Design outcomes

Primary

MeasureTime frame
Incidence of pneumococcal pneumonia requiring hospitalisation, confirmed by blood culture or PCR analysis of bloodSubjects will be enrolled on admission to hospital and followed for the duration of hospitalization (median duration 6 days)
Incidence of pneumococcal meningitis, confirmed by culture or PCR on cerebro-spinal fluidSubjects will be enrolled on admission to hospital and followed for the duration of hospitalization (median duration 6 days)

Secondary

MeasureTime frame
Incidence of suspected pneumonia requiring hospitalisation with reduced oxygen saturation (<90%)Subjects will be enrolled on admission to hospital and followed for the duration of hospitalization (median duration 6 days)
Incidence of radiologically confirmed pneumonia requiring hospitalisationSubjects will be enrolled on admission to hospital and followed for the duration of hospitalization (median duration 6 days)
Incidence of acute meningitis of other bacterial etiologySubjects will be enrolled on admission to hospital and followed for the duration of hospitalization (median duration 6 days)
Incidence of pneumonia of other bacterial or viral etiology requiring hospitalisationSubjects will be enrolled on admission to hospital and followed for the duration of hospitalization (median duration 6 days)
Incidence of suspected pneumonia requiring hospitalisation with elevated C-reactive protein serum concentration (<40mg/l)Subjects will be enrolled on admission to hospital and followed for the duration of hospitalization (median duration 6 days)

Countries

Togo

Contacts

Primary ContactMakawa-Sy Makawa, MD
makmaksy@yahoo.fr+228-921 29 31
Backup ContactHaoua Tall, PharmD MPH
htall@aamp.org+226-50300406

Outcome results

None listed

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