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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00294021
Other study ID # CAIH-LTNP
Secondary ID
Status Completed
Phase N/A
First received February 17, 2006
Last updated September 25, 2012
Start date March 2006
Est. completion date April 2008

Study information

Verified date September 2012
Source Johns Hopkins Bloomberg School of Public Health
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Pneumococcus is a major cause of morbidity and mortality. In 2000, a pneumococcal conjugate vaccine (PCV) was licensed for use in children and is now part of the routine childhood vaccine schedule. PCV is known to reduce invasive disease and protect against nasopharyngeal (NP) acquisition of vaccine serotype pneumococci; it also results in an increased risk of nonvaccine serotype carriage. This study proposes to assess the longterm impact of vaccine on NP carriage in a setting where there is intense antibody pressure on the ecology of the pneumococcus. A cross sectional study of pneumococcal NP colonization among American Indian children will be combined with surveillance for invasive disease in the same population. The purpose is to determine the impact of community wide PCV use on NP colonization and the relationship with invasive disease. This longterm safety issue needs to be assessed to fully evaluate the impact of vaccine on NP ecology and invasive disease.


Description:

There are four specific aims for this study: (1) to determine the overall and serotype specific prevalence and incidence of pneumococcal carriage among children and adults at high risk for carriage and disease in the era of routine pneumococcal conjugate vaccine (PCV) use compared with those measures in the same population prior to use of PCV vaccine; (2) to characterize the intrafamilial NP transmission of clones among those living with children less than 8 years of age; (3) to determine the immune correlates of protection from serotype specific pneumococcal carriage among individuals immunized and not immunized with PCV; and (4) to determine the relative invasiveness of serotypes of pneumococcus during an era of widespread PCV use and compare this to the relative invasiveness of serotypes prior to routine use of PCV.


Recruitment information / eligibility

Status Completed
Enrollment 1000
Est. completion date April 2008
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria for the Family to Participate.

1. At least one parent is a member of the Navajo or White Mountain Apache Tribe

2. Family home is on or near the Navajo or Apache reservation

3. At least one child in the household is 8 years of age or younger (minimum age of eligibility: birth)

4. At least one child in the household is fully immunized with Prevnar.

5. At least two people in the household will participate in the study

6. Willingness to participate for a 6-month time period

Exclusion Criteria for the Family to Participate.

1. Family will be moving off reservation during the study period

Inclusion Criteria for Individuals.

1. Living in the household

2. Willing to participate for a 6-month time period

Exclusion Criteria for Individuals.

1. Congenital anomalies of the nasopharynx

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Johns Hopkins Center for American Indian Health Chinle, Fort Defiance, Whiteriver, AZ; Gallup, Shiprock, NM Arizona

Sponsors (6)

Lead Sponsor Collaborator
Johns Hopkins Bloomberg School of Public Health Centers for Disease Control and Prevention, Finnish Public Health Institute, Grand Challenges in Global Health, Institute of Child Health, Thrasher Research Fund

Country where clinical trial is conducted

United States, 

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