Study to Eliminate Hib Carriage in Rural Alaska Native Villages

Phase 4

Completed

• Conditions: Haemophilus Influenzae Type B; Carrier State

• Registration Number: NCT00153556
• Lead Sponsor: Centers for Disease Control and Prevention

Brief Summary

Hib disease rates in rural Alaska before introduction of HIb conjugate vaccine were among the highest in the world. Since vaccine introduction, rates have fallen by 90% but the disease has not been eliminated. This study is designed to test one possible means of eliminating Hib carriage and thus to eliminate person to person transmission and invasive disease.

The objective of this study is to evaluate the effectiveness of community-wide use of Hib conjugate vaccine for eliminating oropharyngeal Hib carriage in rural Alaska villages.

Secondary objectives include:

* Determine risk factors for Hib OP carriage including demographic characteristics, and immunologic characteristics (antibody level and function). This will be accomplished through a case-control study described below.

* Measure antibody response to Hib conjugate vaccine among adults who have not previously received Hib vaccine. This will be accomplished through a cohort study of participating adults in the vaccine intervention communities.

Detailed Description

This was a pilot intervention to assess the feasibility of using Hib conjugate vaccine to eliminate Hib carriage in rural Alaska villages, with three villages to serve as a comparison group. WE performed community-wide surveys of Hib carriage by recruiting volunteers for throat cultures to establish a baseline rate of Hib carriage for each community. Then Hib carriers were offered chemoprophylaxis to clear Hib from their throats. In the vaccine intervention communities, a single dose of Hib conjugate vaccine was offered to persons of all ages. This was followed by a second community-wide Hib carriage survey after one year to assess the effectiveness of the intervention.

Study Timeline

• Study Start: 2001-09
• Study Completion: 2003-11
• Status Verified: 2005-09
• Study First Submitted: 2005-09-08
• Study First Submitted QC: 2005-09-08
• Last Update Submitted: 2005-09-08
• Study First Posted: 2005-09-12
• Last Update Posted: 2005-09-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 3200

Inclusion Criteria

• All village residents are eligible for Hib colonization survey
• All residents of selected villages eligible for vaccine study except as noted below.

Exclusion Criteria

• For receipt of vaccine:
• history of allergic reaction to Hib vaccine or components
• Age < 24 months and not due for Hib vaccine according to childhood immunization schedule
• Age > 24 months and have received HIb vaccine within past year
• Pregnant

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Change in community-wide oropharyngeal Hib colonization one year after administration of a single dose of Hib vaccine to all willing community members in 3 villages vs. change in HIb colonization in 3 village where Hib vaccine was used routinely

Secondary Outcome Measures

Name	Time	Method
- Safety of HIb vaccine given to adults
- Anti-PRP antibody/ avidity/ serum bacteriocidal activity among adult vaccine recipients, Hib colonized persons and age-matched controls
- Risk factors for Hib colonization

Trial Locations

Locations (1)

CDC Arctic Investigations Program; 🇺🇸 Anchorage, Alaska, United States