ACTIVCOQ: Pediatric Pertussis in Ambulatory Settings

Sponsor
Association Clinique Thérapeutique Infantile du val de Marne (Other)
Overall Status
Recruiting
CT.gov ID
NCT04807712
Collaborator
GlaxoSmithKline (Industry), Sanofi (Industry), Merck Sharp & Dohme LLC (Industry)
874
1
276
3.2

Study Details

Study Description

Brief Summary

Since 2002, Whooping cough surveillance in pediatric private practice has been set up in France. The results of the first years, 2002-2006, have confirmed the effectiveness of the Pertussis whole-cell (Pw) vaccine and in particular the duration of protection of 9/10 years. After evaluating cases in children vaccinated with Pw vaccines, the study aims today to analyze cases in children vaccinated with Pertussis acellular (Pa) vaccines used since 2002/2003 and to assess, on an outpatient basis, the impact of new vaccine recommendations in France (in 2013, introduction of a 2 + 1 schedule - 8 weeks, 4 months and a 11-month recall - and a 6-year recall, and in 2014, update in the recommendations of exams to be prescribed based on the child's age and vaccination status).

Condition or Disease Intervention/Treatment Phase
  • Other: non interventionnal study

Detailed Description

The whooping cough surveillance objectives are :
  • to follow the duration of protection of the Ca vaccines in the context of modifications of the vaccine recommendations

  • to describe the clinical characteristics of a population vaccinated with several boosters

  • to adapt complementary examinations for diagnostic purposes (culture, PCR, serology) according to the evolution of scientific knowledge

  • to monitor B. parapertussis infections

  • to train laboratories with nasopharyngeal aspiration

  • to monitor the evolution of the bacterial species All children aged 0-18 years, in whom the diagnosis of pertussis is mentioned and for which a biological check-up is requested, are included, except asymptomatic children with confirmed family case.

In case of suspected pertussis, real-time PCR and / or culture and / or (rarely) serology is / are still prescribed to the patient and / or his entourage.

Selected Pediatricians from the ACTIV group and the AFPA working in an outpatient clinic, located in different places in France, are participating in this network since 2001. The clinical evolution and the results of the examinations are transcribed on a case report form. The data are collected, firstly, during the visit where the diagnosis of whooping cough is suspected and a biological assessment requested (patient's medical history, clinical data, vaccination status and dates, as well as the search for a contaminated/contaminator) and secondly during the follow-up visit (results of the biological check-up and diagnosis, antibiotics potentially prescribed, and supplement data of the entourage, except in case of diagnosis of pertussis not retained).

All evaluations made by the pediatricians are regularly reviewed during meetings, and final diagnoses used are:

  • biological pertussis

  • epidemiological pertussis

  • not evaluable

  • lost of follow up

  • no whooping cough

Study Design

Study Type:
Observational
Anticipated Enrollment :
874 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
National Surveillance of Pediatric Pertussis in Ambulatory Settings
Actual Study Start Date :
Jan 1, 2002
Actual Primary Completion Date :
Jan 1, 2002
Anticipated Study Completion Date :
Jan 1, 2025

Outcome Measures

Primary Outcome Measures

  1. Duration of pertussis vaccines protection [at inclusion]

    Evaluate the duration of protection of the Ca vaccines

Secondary Outcome Measures

  1. Clinical characteristics of pertussis [at inclusion]

    Describe the clinical characteristics of a population vaccinated

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Day to 18 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • All children under 18 years old with a pertussis diagnosis is suspected and a biological exam is requested
Exclusion Criteria:
  • children without symptoms with a houshold confirmed case

  • cases for which the pertussis diagnosis was not suspected by the pediatrician

Contacts and Locations

Locations

Site City State Country Postal Code
1 ACTIV Créteil France 94000

Sponsors and Collaborators

  • Association Clinique Thérapeutique Infantile du val de Marne
  • GlaxoSmithKline
  • Sanofi
  • Merck Sharp & Dohme LLC

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Association Clinique Thérapeutique Infantile du val de Marne
ClinicalTrials.gov Identifier:
NCT04807712
Other Study ID Numbers:
  • ACT0606
First Posted:
Mar 19, 2021
Last Update Posted:
Mar 23, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Association Clinique Thérapeutique Infantile du val de Marne
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 23, 2021