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Effect of topical Dorzolamide and Latanoprost on Refraction

Long-term effect of topical Dorzolamide and Latanoprost on Refraction in patients with primary open-angle glaucoma

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013052813505N1
Enrollment
88
Registered
2014-09-07
Start date
2013-06-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

glaucoma. Primary open-angle glaucoma

Interventions

Intervention 1: Control: Including patiens who will receive 0.005% latanoprost eye drops once a day for 6±1 weeks. Intervention 2: Control: including patients who will receive 2% dorzolamide eye drop
Treatment - Drugs
Control: Including patiens who will receive 0.005% latanoprost eye drops once a day for 6±1 weeks.
Control: including patients who will receive 2% dorzolamide eye drops three times a day for 6±1 weeks

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 149 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patients with open angle glaucoma; older than 16; with eye pressure of 21 to 30 mm Hg which have not taken any treatment. Exclusion criteria: previous use of systemic or topical dorsolamide; using contact lens since 1 month ago; taking sulfa drug since 1 month ago; lactation; pregnancy (pregnancy reduce eye pressure and increase cornea thickness); cataract; any kind of eye surgery; CD/disc more than 0.8; best visually by less than 20/40 (with using Pin Hole); any neuropathy, any severe damage to visual field; and also any increase in eye pressure more than 30 mm Hg during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Refraction. Timepoint: 2 and 6±1weeks. Method of measurement: Autorefractometr.

Secondary

MeasureTime frame
Visual acuity, thickness of lens and cornea and depth of anterior chamber. Timepoint: 2 and 6±1weeks. Method of measurement: Visual acuity with Snelen chart, thickness of lens and cornea and depth of anterior chamber by IOL Master.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarges Moslehi Moghaddam

Shahid Beheshti University of Medical Sciences

nana.opt@gmail.com+98 21 7729 9258

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026