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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01590381
Other study ID # IDF 1047-2011
Secondary ID
Status Recruiting
Phase N/A
First received May 1, 2012
Last updated May 1, 2012
Start date December 2011
Est. completion date April 2013

Study information

Verified date May 2012
Source Medical Corps, Israel Defense Force
Contact Michael Hartal, MD
Phone +972-3-7374137
Email Mhuerta2@gmail.com
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess HBV immunity and institute policy regarding the Hepatitis B vaccination practices in the IDF among a cohort that was vaccinated during infancy.


Description:

The study population will consist of both males and females who were born after January 1st 1992, who are in medical training at the Medical Corps Training Base. Demographic information will be obtained through a questionnaire given to the soldiers in the study , as well as the IDF computerized personnel information database.

This study is designed to determine HBV vaccination policy among new HCWs in the IDF, who were vaccinated during infancy. This population was recruited to the IDF since the second half of 2010. Therefore, it is necessary to conduct this study on new HCWs that will be receiving the routine HBV vaccination and that will be at risk for HBV infection in the future due to their occupation in the army (HCWs, etc).


Recruitment information / eligibility

Status Recruiting
Enrollment 545
Est. completion date April 2013
Est. primary completion date January 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

1. Soldiers born on or after January 1st, 1992

2. Soldiers taking part in a medical training course

3. Soldiers that signed an informed consent form

Exclusion Criteria:

1. Born before January 1st, 1992

2. Soldiers with previous known infection with HBV

3. Soldiers with documented evidence of immunity against HBV

4. Soldiers that refuse to participate in the study

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Israeli Defense Forces Tel Aviv

Sponsors (1)

Lead Sponsor Collaborator
Medical Corps, Israel Defense Force

Country where clinical trial is conducted

Israel, 

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