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24-hour intraocular pressures with brimonidine purite versus dorzolamide added to latanoprost in primary open-angle glaucoma subjects.

AbstractOBJECTIVE:
To evaluate the 24-hour efficacy of brimonidine purite versus dorzolamide, each added to latanoprost.
DESIGN:
Double-masked, 2-center, prospective, crossover comparison.
PARTICIPANTS:
Primary open-angle glaucoma (POAG) subjects.
METHODS:
Subjects were randomized to brimonidine purite or dorzolamide, each given twice daily, for the first 6-week treatment period after a 6-week latanoprost run-in. Subjects began the opposite treatment for the second 6-week period after a 6-week latanoprost-only treatment between periods. Intraocular pressure (IOP) was measured at 8 am, 12 pm, 4 pm, 8 pm, 12 am, 4 am, and 8 am at each baseline and at the end of each treatment period. This study provided an 80% power that a 1.5-mmHg difference could be excluded between groups if 27 subjects completed the study. A standard deviation (SD) of 2.8 mmHg was assumed.
MAIN OUTCOME MEASURES:
Twenty-four-hour efficacy of intraocular pressures of brimonidine purite versus dorzolamide, each added to latanoprost.
RESULTS:
In 31 completed subjects, the baseline mean diurnal 24-hour IOP (+/- SD) was 19.0+/-1.7 mmHg for brimonidine purite and 19.0+/-1.6 mmHg for dorzolamide (P = 0.52). The 8 am IOP after 6 weeks of therapy was 18.4+/-2.1 mmHg for brimonidine purite and 18.9+/-1.9 mmHg for dorzolamide (P = 0.40). The mean diurnal IOP was 16.9+/-1.5 mmHg for brimonidine purite and 16.8+/-1.5 mmHg for dorzolamide (P = 0.66). Dorzolamide caused a more bitter taste (P = 0.01) than brimonidine purite.
CONCLUSIONS:
This study suggests that brimonidine purite and dorzolamide, added to latanoprost, have similar efficacy and safety in POAG or ocular hypertensive subjects.
AuthorsAnastasios G P Konstas, Costas H Karabatsas, Nikolaos Lallos, Nikolaos Georgiadis, Aikaterini Kotsimpou, Jeanette A Stewart, William C Stewart
JournalOphthalmology (Ophthalmology) Vol. 112 Issue 4 Pg. 603-8 (Apr 2005) ISSN: 1549-4713 [Electronic] United States
PMID15808251 (Publication Type: Clinical Trial, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Antihypertensive Agents
  • Prostaglandins F, Synthetic
  • Quinoxalines
  • Sulfonamides
  • Thiophenes
  • Brimonidine Tartrate
  • Latanoprost
  • dorzolamide
Topics
  • Aged
  • Antihypertensive Agents (adverse effects, therapeutic use)
  • Brimonidine Tartrate
  • Circadian Rhythm
  • Cross-Over Studies
  • Double-Blind Method
  • Drug Therapy, Combination
  • Female
  • Glaucoma, Open-Angle (drug therapy)
  • Humans
  • Intraocular Pressure (drug effects)
  • Latanoprost
  • Male
  • Prospective Studies
  • Prostaglandins F, Synthetic (adverse effects, therapeutic use)
  • Quinoxalines (adverse effects, therapeutic use)
  • Safety
  • Sulfonamides (adverse effects, therapeutic use)
  • Thiophenes (adverse effects, therapeutic use)
  • Visual Acuity

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