NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
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
Health condition(s) or Problem(s) studiedspring hay fever
Date of first enrollment2007/02/01
Target sample size40
Countries of recruitmentJapan
Study typeObservational
Intervention(s)

Outcome(s)

Primary Outcomeglobal assessment of Rtime operationality
Secondary Outcomedrug compliance, follow rate, sleepness score, global assessment of symptom, consent rate

Key inclusion & exclusion criteria

Age minimumNot applicable
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteriawho 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

Contact

public contact
Name
Address Japan
Telephone
E-mail
Affiliation Oita University Clinical Pharmacology Center
scientific contact
Name ISAMU HORIKAWA
Address 270 Okyozuka, Nonoichi , ISHIKAWA Japan
Telephone 076-240-0600
E-mail
Affiliation Horikawa Clinic otorhinolaryngology