NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000036705

Registered date:10/05/2019

An observational study focusing on the changes of the upper eyelid sulcus after switching from FP receptor agonist to omidenepag isoproryl ophthalmic solution

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedGlaucoma, ocular hypertension
Date of first enrollment2019/05/31
Target sample size30
Countries of recruitmentJapan
Study typeObservational
Intervention(s)

Outcome(s)

Primary OutcomeChanges of findings and subjective symptom and quality of life about the upper eyelid sulcus
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1) a patient with aphakic or pseudophakic eyes 2) a patient with hypersensitivity to Omidenepag isopropyl ophthalmic solution 0.002%

Related Information

Contact

public contact
Name Rei Sakata
Address Yotsuya Mitsuke building 3F, 1-1-2, Yotsuya, Shinjyuku-ku, Tokyo Japan 160-0004
Telephone 03-3355-4281
E-mail reisakata-tky@umin.ac.jp
Affiliation Yotsuya Shirato Eye Clinic Ophthalmology
scientific contact
Name Makoto Aihara
Address Yotsuya Mitsuke building 3F, 1-1-2, Yotsuya, Shinjyuku-ku, Tokyo Japan
Telephone 03-3355-4281
E-mail aihara-tky@umin.net
Affiliation Yotsuya Shirato Eye Clinic Ophthalmology