UMIN ID: UMIN000000612
Registered date:17/07/2007
Preliminary study of close monitoring for outpatients of spring hay fever using newly invented support system, Rtime.
Basic Information
Recruitment status | Complete: follow-up complete |
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Health condition(s) or Problem(s) studied | spring hay fever |
Date of first enrollment | 2007/02/01 |
Target sample size | 40 |
Countries of recruitment | Japan |
Study type | Observational |
Intervention(s) |
Outcome(s)
Primary Outcome | global assessment of Rtime operationality |
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Secondary Outcome | drug compliance, follow rate, sleepness score, global assessment of symptom, consent rate |
Key inclusion & exclusion criteria
Age minimum | Not applicable |
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Age maximum | Not applicable |
Gender | Male and Female |
Include criteria | |
Exclude 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. |
Related Information
Primary Sponsor | Oita University |
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Secondary Sponsor | |
Source(s) of Monetary Support | NPO HEART |
Secondary ID(s) |
Contact
public contact | |
Name | |
Address | Japan |
Telephone | |
Affiliation | Oita University Clinical Pharmacology Center |
scientific contact | |
Name | ISAMU HORIKAWA |
Address | 270 Okyozuka, Nonoichi , ISHIKAWA Japan |
Telephone | 076-240-0600 |
Affiliation | Horikawa Clinic otorhinolaryngology |