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Comparison Between the Effectiveness of Fixed Combinations of Prostaglandin Analogues

Comparison Between the Effectiveness of Fixed Combinations of Prostaglandin Analogues Regarding Intraocular Pressure Control

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610001034022
Enrollment
60
Registered
2010-11-24
Start date
2010-10-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Patients with primary open angle glaucoma or ocular hypertensio will be treated with fixed combinations of prostaglandin analogues plus beta blocker. They will be follow for 60 days. Intraocular pressure will be compared. Comparisons beteween groups and with baseline.

Interventions

Patients will use fixed combinations of prostaglandin analogues plus topical beta blockers available on market during 60 days. Patients will be divided in three groups. Each group will recieve one drug. Intraocular pressure will be compared. If using drugs prior to study, a washout period of 30 days will be necessary. Half of patients will receive the drug at mornig (8 a.m.) and half at night (8 p.m.). After 30 days they will change the time to use the drug (crossover regarding the instillation

Patients will use fixed combinations of prostaglandin analogues plus topical beta blockers available on market during 60 days. Patients will be divided in three groups. Each group will recieve one drug. Intraocular pressure will be compared. If using drugs prior to study, a washout period of 30 days will be necessary. Half of patients will receive the drug at mornig (8 a.m.) and half at night (8 p.m.). After 30 days they will change the time to use the drug (crossover regarding the instillation time), without washout between these change. The drugs are: Xalacom (latanoprost 0.005%/timolol 0.5%) eye drop once day; Ganfort (bimatoprost 0.03%/timolol 0.5%) eye drop once day; and Duotrav (travoprost 0.004%/timolol 0.5%) eye drop once day.

Sponsors

Enyr Saran Arcieri
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

Intra ocular pressure over 21 MMHG

Exclusion criteria

Pregnancy

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026