Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/67333
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMishra, Astha-
dc.contributor.authorMuthuswamy, Pooja-
dc.contributor.authorDass, Shankar-
dc.contributor.authorSharma, Bunty-
dc.contributor.authorSharma, Ujjawal-
dc.date.accessioned2026-03-02T08:54:42Z-
dc.date.available2026-03-02T08:54:42Z-
dc.date.issued2026-02-
dc.identifier.issn0975-1009 (Online) ; 0019-5189 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/67333-
dc.description141-147en_US
dc.description.abstractThis study reports on the effect of lowering intraocular pressure with the combination drug therapies, Ripasudil with Dorzolamide, given in conjunction with prostaglandin analogues (PGAs) in patients diagnosed with glaucoma. The study was conducted on a cohort of 120 glaucoma patients who required additional therapeutic interventions beyond latanoprost monotherapy to achieve optimal intraocular pressure (IOP) control. The IOP was measured weekly for 12 weeks during the study to evaluate the effectiveness of the drugs used in combination therapy. This compound, known as Ripasudil hydrochloride hydrate, or K-115, is a new class of Rho kinase inhibitors that have gained special interest because they decrease IOP without a well-characterised mechanism; its main advantage lies in enhancing aqueous outflow at the trabecular meshwork. The findings show that the IOP-controlling efficacy of Ripasudil is equal to that of Dorzolamide in combination therapy. In Group A, ocular discomfort was reported by 6 patients (10%), blurred vision by 3 patients (5%), and systemic side effects by 1 patient (1.7%). In Group B, ocular discomfort occurred in 4 patients (6.7%), and blurred vision occurred in 2 patients (3.3%), while no systemic adverse effects were reported. The overall incidence of adverse events was 16.7% in Group A and 10% in Group B, but this difference was not statistically significant (P > 0.05). This outcome underlines the role of Ripasudil as a potential substitute for patients who need supplementary IOP-lowering treatment over PGA monotherapy. In addition, the novel mechanism of Ripasudil presents some benefits, especially for patients with minimal response to carbonic anhydrase inhibitors. This study underscores the need to explore innovative adjunctive treatments for glaucoma and supports the clinical utility of Ripasudil as a safe and effective option when combined with prostaglandin analogues to achieve optimal IOP control.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJEB Vol.64(02) [February 2026]en_US
dc.subjectRipasudilen_US
dc.subjectDorzolamideen_US
dc.subjectIntraocular Pressureen_US
dc.subjectProstaglandinen_US
dc.subjectAnaloguesen_US
dc.titleComparison of the impact of Ripasudil and Dorzolamide on intraocular pressure in patients on prostaglandin analoguesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijeb.v64i02.25361en_US
Appears in Collections:IJEB Vol.64(02) [February 2026]

Files in This Item:
File Description SizeFormat 
IJEB Vol. 64 (02) 141-147.pdf814.72 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.