American Journal of Ophthalmology
Volume 149, Issue 4 , Pages 661-671.e1 , April 2010

Twelve-Month, Randomized, Controlled Trial of Bimatoprost 0.01%, 0.0125%, and 0.03% in Patients with Glaucoma or Ocular Hypertension

  • L. Jay Katz

      Affiliations

    • Wills Eye Hospital, Philadelphia, Pennsylvania
    • Corresponding Author InformationInquiries to L. Jay Katz, Glaucoma Service, Wills Eye Hospital, 840 Walnut Street, Suite 1110, Philadelphia, PA 19107
  • ,
  • John S. Cohen

      Affiliations

    • Cincinnati Eye Institute, Cincinnati, Ohio
  • ,
  • Amy L. Batoosingh

      Affiliations

    • Allergan, Inc, Irvine, California
  • ,
  • Carlos Felix

      Affiliations

    • Allergan, Inc, Irvine, California
  • ,
  • Vincent Shu

      Affiliations

    • Allergan, Inc, Irvine, California
  • ,
  • Rhett M. Schiffman

      Affiliations

    • Allergan, Inc, Irvine, California

,Accepted 1 December 2009.

References 

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  21. Whitson JT, Cavanagh HD, Lakshman N, Petroll WM. Assessment of corneal epithelial integrity after acute exposure to ocular hypotensive agents preserved with and without benzalkonium chloride. Adv Ther. 2006;23:663–671
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  23. Kahook MY, Noecker RJ. Comparison of corneal and conjunctival changes after dosing of travoprost preserved with sofZia, latanoprost with 0.02% benzalkonium chloride, and preservative-free artificial tears. Cornea. 2008;27:339–343
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  29. Brandt JD, Beiser JA, Gordon MO, Kass MA Ocular Hypertension Treatment Study (OHTS) Group. Central corneal thickness and measured IOP response to topical ocular hypotensive medication in the Ocular Hypertension Treatment Study. Am J Ophthalmol. 2004;138:717–722
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PII: S0002-9394(09)00906-4

doi: 10.1016/j.ajo.2009.12.003

American Journal of Ophthalmology
Volume 149, Issue 4 , Pages 661-671.e1 , April 2010