Bimatoprost 0.03% Versus Travoprost 0.004% in Patients Currently on Latanoprost 0.005%

Study Identifier
MA-LUM01
CT.gov Identifier
NCT00440011
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Study Details

Medical Condition
  • Glaucoma - Other
  • Ocular Hypertension
    • Study Drug
  • bimatoprost 0.03% eye drops
  • travoprost 0.004% eye drops
    • Phase
    Phase 4
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Glaucoma or ocular hypertension in both eyes * Currently being treated with latanoprost 0.005% daily and in need of additional IOP-lowering * Best-corrected visual acuity of 20/100 or better in each eye * Visual field within 6 months of study entry
    Exclusion Criteria:
    * Secondary glaucoma * Active intraocular inflammation or macular edema * Intraocular surgery or laser surgery within the past 3 months

    Protocol Summary

    Patients with glaucoma or ocular hypertension currently being treated with latanoprost 0.005%, and in need of additional IOP lowering, will be randomized to receive either bimatoprost 0.03% or travoprost 0.004% in place of latanoprost 0.005%

    Study Locations

    Location
    Status
    Location
    San Diego, California, United States
    Status
    Not applicable