The Protection Effect of Speeda® Rabies Vaccine for Human Use

Beijing Center for Disease Control and Prevention37 enrolled

Overview

The objective of this study was to achieve the post-marketing protective effect research of Speeda® rabies vaccine for human use from Chengda Bio.

When found the injury who is bitten by the animal to three-level, the investigators would enroll the participant after explaining the protection and making him signed the informed consent. The patient would inject rabies vaccine as follow the national regulation, meanwhile the investigators would get the blood samples to detect whether the man-killer carries the rabies virus.

Study Type

INTERVENTIONAL

Allocation

Purpose

PREVENTION

Masking

NONE

Enrollment

Conditions

Rabies Vaccine Allergy

Interventions

rabies vaccineBIOLOGICAL

Injection on day 0、7、21

Eligibility

Sex: ALLHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Parent/legal acceptable representatives of children or the adult participants are willing and able to understand the protocol requirements and provide informed consent signed * Participant is considered to be in good health including the body and mental status on the basis of reported medical history and limited physical examination and live in local ≥ 12 months before injured * The man-killer could found and detect whether it carries the virus Exclusion Criteria: * Known bleeding disorder or suspected impairment of immunologic function, or receipt of immunosuppressive therapy or immunoglobulin since birth * Apply passive immunity preparation

Locations (1)

Hunan Centers for Disease Control and Prevention

Changsha, Hunan, China

Outcomes

Primary Outcomes

Observation of the subject after injured by the animals carrying the virus

Whether or when would the patients develop symptoms after injured by the animals carrying the virus

Time frame: 2 years

Data from ClinicalTrials.gov

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