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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03983616
Other study ID # SIIP
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 2014
Est. completion date April 2020

Study information

Verified date June 2019
Source University Hospital, Limoges
Contact Marie-Cécile PLOY, MD
Email marie-cecile.ploy@unilim.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Given the frequency and severity of invasive pneumococcal infections and questions about the place of VPC-13 in the prevention of pneumococcal infections in adults based on the presence of risk factors, current laboratory surveillance should be supplemented with data on the clinical features of adult invasive pneumococcal infections (IPI) cases. In particular it is necessary to collect for these cases, the clinical forms, the severity and the existence of risk factors and to make the link between these characteristics and those strains of pneumococci responsible for the IPI in particular, their serotype. The follow-up of the evolution of the cases according to the presence of risk factors, their clinical form and their serotype coverage (vaccine strain or not) must to guide recommendations for adult VPC-13 and to monitor the effects of VPC-13 vaccination recommendations. These effects are indirect, linked to the effect of vaccination of children with VPC-13 since 2010, which modifies the serotypes responsible for infections in vaccinated and unvaccinated patients, and the direct effects of possible use of the conjugate vaccine in adults (according to the recommendations that will be given by the Vaccination Technical Committee of the High Council of Public Health). The project is based on the existing network of 23 Regional Pneumococcal Observatories (ORP) located in metropolitan France and the network of infectious diseases by completing the microbiological collection of strains of pneumococci isolated from invasive infections in adults by a clinical collection in hospitals or voluntary clinics where the laboratory participates in the ORP. Given the establishment in 2012 of an adult bacterial meningitis observatory, to which the ORP are associated, this project does not include the surveillance of pneumococcal meningitis in adults.


Recruitment information / eligibility

Status Recruiting
Enrollment 1560
Est. completion date April 2020
Est. primary completion date April 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years old patients or older hospitalized with invasive pneumococcal infection confirmed by isolation of a strain from a usually sterile site: blood or pleural fluid

Exclusion Criteria:

- Pneumococcal meningitis identified by pneumococcal isolation or pneumococcal positive polymerase chain reaction (PCR) in cerebrospinal fluid

Study Design


Locations

Country Name City State
France Service de Virologie Limoges

Sponsors (5)

Lead Sponsor Collaborator
University Hospital, Limoges CNRP, INVS, ORP, SPILF

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of invasive pneumococcal infections identify the frequency of invasive pneumococcal infections in function of the presence of risk factors Day 0
Secondary Weight of invasive pneumococcal infections measure the weight of invasive pneumococcal infections based on the presence of risk factors and immunization or not Day 0
Secondary Number of Invasive Pneumococcal Infections in Adults monitor the epidemiology of Invasive Pneumococcal Infections in Adults according to strategies for the use of VPC-13 and VPS-23 vaccines in children and adults Day 0
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