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Efficacy and Adherence of Xalacom Combination Therapy in Glaucoma Patients Switching from a Multi-Drug Therapy (PG and beta blocker medication)

Efficacy and Adherence of Xalacom Combination Therapy in Glaucoma Patients Switching from a Multi-Drug Therapy (PG and beta blocker medication) - Efficacy and Adherence of Xalacom switching from a Multi-Drug Therapy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007042
Enrollment
50
Registered
2012-01-10
Start date
2011-02-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma, ocular hypertension

Interventions

12 Weeks administration of Xalacom to the patients who are treated with concomitant application of two or more anti-glaucoma drugs including a PG analogs and a beta blocker over four weeks

Sponsors

Department of Ophthalmology, Kitasato University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients of glaucoma or ocular hypertension treated with applying a PG analogs and a beta blocker concomitantly 1) Patients who were fully informed and gave their written informed consent to this study 2) IOP in a range of 12 to 21 mmHg 3) visual acuity is over 0.7 4) A doctor decides to switch from such drugs to Xalacom combination eye drops

Exclusion criteria

Exclusion criteria: 1) Patients in whom the studied drug is "Contraindication" 2) Patients in whom the studied drug is "Careful Administration" 3) Patients with corneal abnormalities that would hinder the measurement of IOP using Goldmann applanation tonometry 4) Patients whose pupils could dilate so insufficiently that it is impossible to observe optic papillae 5) Patients with a history of a laser treatment 6) Patients with uveititis, an eye injury, an infectious eye disease or an inflammatory eye disease as an accompanying disease 7) Patients with a history of narrow angle that may be closed, or acute angle closure 8) Patients with a retinal disease that might affect the visual field of either or both eyes, as an accompanying disease 9) Patients with a history of an infectious disease within four weeks of participation in this study 10) Patients who had been using any drug that might have a systemic effect that affects intraocular pressure 11) Patients assessed as unsuitable for participation in the study by the investigator and/or subinvestigators

Design outcomes

Primary

MeasureTime frame
Intra ocular pressure of 12Weeks after switching from concomitant therapy

Secondary

MeasureTime frame
Change rate of intraocular pressure, adherence, safety

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026