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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04725669
Other study ID # UHID-06
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 15, 2021
Est. completion date September 8, 2022

Study information

Verified date February 2021
Source University Hospital for Infectious Diseases, Croatia
Contact Goran Tešovic
Phone +385914012605
Email gtesovic@bfm.hr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pertussis is a vaccine preventable disease caused by Bordetella pertussis. Older children and adolescents with pertussis continue to be a significant source of infection for incompletely vaccinated infants who are in harm for developing severe disease. The primary objective of our study is to estimate the duration of protection elicited by the current vaccination schedule against pertussis in Croatia.


Recruitment information / eligibility

Status Recruiting
Enrollment 1500
Est. completion date September 8, 2022
Est. primary completion date June 14, 2022
Accepts healthy volunteers No
Gender All
Age group 6 Years to 18 Years
Eligibility Inclusion Criteria: - children and adolescents from 6 to 18 years of age treated through Emergency room and/or Day hospital of Pediatric Infectious Diseases Department at UHID; - appropriate vaccination with pertussis component containing vaccine by date and at the appropriate time, according to Croatian NIP proven by insight in the Vaccination Record Card - written informed consent obtained from the subject's parent or caregiver, as well as from participants = 16 years old. Exclusion Criteria: - children under 6 years - children and adolescents with acute respiratory symptoms - children and adolescents with pertussis-like illness within 12 months - children and adolescents with unknown, uncompleted or irregular vaccination record - inpatients - children and adolescents with immunodeficiencies

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
ELISA IgG Testkit
All samples will be tested for IgG antibody level to pertussis toxin using a commercial Bordetella pertussis ELISA IgG Testkit in accordance to the manufacturers' protocol in the laboratory at the University Hospital for Infectious Diseases in Zagreb.

Locations

Country Name City State
Croatia University Hospital for Infectious Diseases "Dr Fran Mihaljevic" Zagreb

Sponsors (2)

Lead Sponsor Collaborator
University Hospital for Infectious Diseases, Croatia Sanofi Pasteur, a Sanofi Company

Country where clinical trial is conducted

Croatia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Waning of vaccine-induced immunity Number of Participants In Each Specific Age Group With Negative Pertussis Toxin IgG Antibody Titre Measured by ELISA IgG Testkit 1 day
Secondary Seroprevalence Prevalence of Pertussis Toxin IgG Antibody Titre At Each Specific Age Subgroup up to 6 months
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