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Objective: PCV effects on S. pneumoniae and S. aureus carriage in a population based study. The major specific aims:
Study design: Annual / Biannual cross-sectional surveillance of nasal S. aureus carriage and nasopharyngeal S. pneumoniae carriage in children and one of their parents.
Full description
Study design: Annual / Biannual cross-sectional surveillance of nasal S. aureus carriage and nasopharyngeal S. pneumoniae carriage in children and one of their parents.
PICR districts: 1. Palestinian Authority (PA) - particularly: Bethlehem, Ramallah and Nabulus. 2. East Jerusalem (EJ) 3. Central Israel (IL) - particularly: Rishon Lezion, Bat Yam, Holon 4. Gaza strip (GZ) - 12 regions including cities/villages in central/northern Gaza.
Study population:
Child (age 0-5y) & Parent who attend clinics (for any reason).
Exclusion criteria:
Parent does not agree to sign informed consent Child or sibling (brother/sister) have already participated.
Both healthy and ill children are screened. No specific exclusion other than the above.
Only one child per family (younger child, if more than one available) and one parent (mother, if both are available).
Sample size per year:
IL: Central Israel (Hashfela District): 400 pairs of child+parent/surveillance EJ: East Jerusalem: 400 pairs of child+parent/surveillance PA: West Bank cities (Ramallah, Bethlehem & Nabulus): 600 pairs of child+parent/surveillance GZ: Gaza strip: 300 pairs of child+parent/surveillance
Study Period:
May-August annually 2009 - 2011 - (Part a). May-August biannually 2014-2016-2018-2020 Current study (Part b).
Screening Procedure:
Swabbing:
Swab transfer to lab:
If swabs are stored overnight before transfer - keep in 40C (fridge). Within 24h swabs must reach the central laboratory (Dr. Regev-Yochay's Lab at Sheba Medical Center).
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12,800 participants in 3 patient groups
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Central trial contact
Ziad Abdeen, PhD; Gili Regev-Yochay, MD
Data sourced from clinicaltrials.gov
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