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Celiprolol versus timolol and placebo: a two week double-blind comparison
J Elman1, J Caprioli, E G Rosanelli
1Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut.
Summary
Celiprolol (5%) and timolol (0.5%) were compared to placebo for glaucoma. Timolol showed a greater reduction in intraocular pressure and a slight decrease in pulse rate, with effects lasting longer than celiprolol.
Area of Science:
- Ophthalmology
- Clinical Pharmacology
Background:
- Primary open-angle glaucoma and ocular hypertension are common conditions affecting intraocular pressure.
- Effective management of intraocular pressure is crucial to prevent optic nerve damage.
Purpose of the Study:
- To compare the efficacy and safety of celiprolol (5%) versus timolol (0.5%) and placebo in patients with primary open-angle glaucoma or ocular hypertension.
- To evaluate the duration of intraocular pressure reduction and systemic effects.
Main Methods:
- A double-blind, randomized study involving 28 patients.
- Treatment with celiprolol (5%), timolol (0.5%), or placebo for two weeks.
- Measurement of intraocular pressure and pulse rate at specified intervals.
Main Results:
- Both celiprolol and timolol reduced intraocular pressure compared to placebo.
- Timolol demonstrated a greater mean decrease in intraocular pressure (7.1 mmHg) than celiprolol (4.4 mmHg) two hours post-instillation.
- The intraocular pressure-lowering effect of timolol was sustained for 12 hours, whereas celiprolol's effect was not.
- Timolol caused a statistically significant but small decrease in pulse rate, not observed with celiprolol.
- Side effects were mild and comparable across all three treatment groups.
Conclusions:
- Timolol (0.5%) appears more effective in reducing intraocular pressure and maintaining this reduction for a longer duration compared to celiprolol (5%) in this patient population.
- Celiprolol (5%) showed a lesser hypotensive effect and did not demonstrate sustained action over 12 hours.
- Both agents were generally well-tolerated, with mild and similar side effect profiles.