Preliminary study of close monitoring for outpatients of spring hay fever using newly invented support system, Rtime.

Preliminary study of close monitoring for outpatients of spring hay fever using newly invented support system, Rtime. - Preliminary study for patient close monitoring system

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000000612

Enrollment

Registered

2007-07-17

Start date

2007-02-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

spring hay fever

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: who can participate with written consent, who is applicable for H1-antagonist treatment, who has spring hay fever, who is outpatient.

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
global assessment of Rtime operationality	—

Secondary

Measure	Time frame
drug compliance, follow rate, sleepness score, global assessment of symptom, consent rate	—

Countries

Japan

Outcome results