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cilostazol and Glaucoma

cilostazol has been researched along with Glaucoma in 1 studies

Glaucoma: An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed)

Research Excerpts

ExcerptRelevanceReference
"To evaluate the pharmacological properties of cilostazol (CLZ), we examined its intraocular pressure (IOP) -lowering effect."7.76Preparation of ophthalmic formulations containing cilostazol as an anti-glaucoma agent and improvement in its permeability through the rabbit cornea. ( Ito, Y; Kurimoto, T; Mimura, O; Murao, T; Nagai, N; Okamoto, N; Takiguchi, Y, 2010)
"To evaluate the pharmacological properties of cilostazol (CLZ), we examined its intraocular pressure (IOP) -lowering effect."3.76Preparation of ophthalmic formulations containing cilostazol as an anti-glaucoma agent and improvement in its permeability through the rabbit cornea. ( Ito, Y; Kurimoto, T; Mimura, O; Murao, T; Nagai, N; Okamoto, N; Takiguchi, Y, 2010)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Okamoto, N1
Ito, Y1
Nagai, N1
Murao, T1
Takiguchi, Y1
Kurimoto, T1
Mimura, O1

Other Studies

1 other study available for cilostazol and Glaucoma

ArticleYear
Preparation of ophthalmic formulations containing cilostazol as an anti-glaucoma agent and improvement in its permeability through the rabbit cornea.
    Journal of oleo science, 2010, Volume: 59, Issue:8

    Topics: 2-Hydroxypropyl-beta-cyclodextrin; Absorption; Animals; Antihypertensive Agents; beta-Cyclodextrins;

2010