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Evaluation of dorzolamide/timolol fixed combination therapy for the patients who need more IOP reduction under PG analogues

Not Applicable
Conditions
primary open angle glaucoma, ocular hypertension
Registration Number
JPRN-UMIN000004596
Lead Sponsor
Department of Ophthalmology, Kyoto Prefectural University of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

1) patients who received any surgical therapy within the past 3 months (incl. laser surgery) 2) difficult to measure IOP with GAT 3) difficult to check the fundus due to the corneal opacity or cataract 4) any patients who are expected to receive any surgical procedures during the study periods 5) contraindication of beta blockers or dorzolamide 6) any allergic history to the timilol or dorzolamide 7) women who are under pregnant or lactation period 8) any one who is considered to be inappropriate for this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
intraocular pressure, ocular and general side effects
Secondary Outcome Measures
NameTimeMethod
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