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Clinical Trials/JPRN-UMIN000011799
JPRN-UMIN000011799
Completed
未知

Efficacy and safety of vaccination of the influenza A (H5N1) Egyptian strain, and searching for the optimal intervals of the primary vaccination. - Efficacy and safety of vaccination of the influenza A(H5N1) Egyptian strain, and searching for the optimal intervals of the primary vaccination. (H5N1_Egypt interval)

Clinical Research Center, National Hospital Organization0 sites140 target enrollmentSeptember 18, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Prevention of influenza
Sponsor
Clinical Research Center, National Hospital Organization
Enrollment
140
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 18, 2013
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Clinical Research Center, National Hospital Organization

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Individuals with the history of Avian Influenza A (H5N1\) virus infection. (obtained from subjects) 2\) Individuals, who had history of anaphylaxis to foods or medicines previously. 3\) Individuals with severe diseases in cardiovascular, blood, respiratory, liver, kidney, digestive or neurological systems in their clinical recording. 4\) Individuals with a history of acute disseminated encephalomyelitis and Guillain\-Barre syndrome in the past. 5\) Individuals participated in a clinical trial within four months (counted from the date of vaccination). 6\) Individuals vaccinated with live vaccine within 27 days, or received a dose of inactivated vaccine within six days (including the day of vaccination). 7\) Individuals received with gamma globulin or blood transfusion within three months, or received the formulation of high dose of gamma globulin therapy (200 mg/kg or more) within six months (including the day of vaccination). 8\)Individuals who are deemed to be inappropriate by the investigator.

Outcomes

Primary Outcomes

Not specified

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