Preliminary study of close monitoring for outpatients of spring hay fever using newly invented support system, Rtime.
Not Applicable
- Conditions
- spring hay fever
- Registration Number
- JPRN-UMIN000000612
- Lead Sponsor
- Oita University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
who is not apllicable for H1 antagonist, who may need systemin steroid treatment, who plans to apply hyposensitization therapy or surgical procedures at the time of consent, who is under the medication which affects to daytime sleepness.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method global assessment of Rtime operationality
- Secondary Outcome Measures
Name Time Method drug compliance, follow rate, sleepness score, global assessment of symptom, consent rate