NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000001180

Registered date:09/06/2008

Correlation between a reduction of intraocular pressure and an increase of compliance with the eye drop guidance

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedglaucoma
Date of first enrollment2008/01/01
Target sample size50
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Period: for 3 months To do the explanation of the disease and guidance for eye drops. Period: for 3 months To do the explanation of the disease.

Outcome(s)

Primary OutcomeThe intraocular pressure at the 3 months.
Secondary Outcome

Key inclusion & exclusion criteria

Age minimumNot applicable
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1)Patients have retinal diseases except optic neuropathy by glaucoma. 2)Patients who had attended other clinical trials 3 months before this IC.

Related Information

Contact

public contact
Name Sasamoto
Address 6-1-219, Chuou, Yonezawa-shi Japan
Telephone 0238-24-3700
E-mail sasamoto@sanyudo.or.jp
Affiliation Sanyudo Hospital dept. Ophthalmology
scientific contact
Name Sasamoto
Address 6-1-219, Chuou, Yonezawa-shi Japan
Telephone 0238-24-3700
E-mail
Affiliation Sanyudo Hospital Department of Ophthalmology