NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000023227

Registered date:20/07/2016

Comparison of the lowering intraocular pressure after trabeculotomy between patients with and without response to Ripasudil.

Basic Information

Recruitment status Pending
Health condition(s) or Problem(s) studied1. Glaucoma 2. Ocular hypertention
Date of first enrollment2016/08/01
Target sample size40
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Trabeculotomy 4 weeks after treatment with Ripasudil.

Outcome(s)

Primary OutcomeIntraocular pressure after trabeculotomy
Secondary OutcomeIntraocular pressure 4 weeks after Ripasudil is initiated C-value of tonography 4 weeks after Ripasudil is initiated C-value of tonography after trabeculotomy

Key inclusion & exclusion criteria

Age minimum16years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteriaPatients who don't agree with the treatment Patients who need emergency glaucoma operation Patient who need trabeculectomy

Related Information

Contact

public contact
Name Suimon Yuka
Address N-15, W-7, Kita-ku, Sapporo, Hokkaido, Japan Japan
Telephone 011-706-5944
E-mail suimonyuka@gmail.com
Affiliation Hokkaido University Graduate School of Medicine Department of Ophthalmology
scientific contact
Name Chin Shinki
Address N-15, W-7, Kita-ku, Sapporo, Hokkaido, Japan Japan
Telephone 011-706-5944
E-mail schin@med.hokudai.ac.jp
Affiliation Hokkaido University Graduate School of Medicine Department of Ophthalmology