Evluation of clinical trial for the rapid diagnostic kit of norovirus
Not Applicable
- Conditions
- orovirus
- Registration Number
- JPRN-UMIN000020102
- Lead Sponsor
- EIKEN CHEMICAL Co., Ltd.
- Brief Summary
As compared to RT-PCR, the sensitivity, secificity and concordance rate is 79.3% (169/213), 99.4%(357/359) and 92.0% (526/572), respectively.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 1000
Inclusion Criteria
Not provided
Exclusion Criteria
The patient applicable to the following items 1)The patient who has participated in other clinical trials 2)The patient judged to be unsuitable by the doctor
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sensitivity, specificity and concordance rate in comparison with the RT-PCR method
- Secondary Outcome Measures
Name Time Method