Travatan Z in Ocular Surface Health in Patients With Open-Angle Glaucoma or Ocular Hypertension

Last updated: July 20, 2012
Sponsor: Alcon Research
Overall Status: Completed

Phase

3

Condition

Glaucoma

Williams Syndrome

Stress

Treatment

N/A

Clinical Study ID

NCT00690794
C-08-03
  • Ages > 18
  • All Genders

Study Summary

The purpose of the study is to compare two ophthalmic solutions in patients with open-angle glaucoma or ocular hypertension.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 18 years or older.

  • Ocular Surface Disease Index (OSDI) score and corneal fluorescein staining score asspecified in protocol.

  • Diagnosis of open-angle glaucoma or ocular hypertension in at least one eye.

  • Intraocular pressure (IOP) controlled with latanoprost 0.005% (XALATAN®) for at leastone continuous month prior to Visit 1.

  • Willing and able to discontinue use of any topical ocular medication other than thestudy medication for the duration of the study, including artificial tears.

  • Best corrected visual acuity of -0.6 logarithm of the Minimum Angle of Resolution (logMAR) or better in each eye.

  • Other protocol-defined inclusion criteria may apply.

Exclusion

Exclusion Criteria:

  • Any medical condition (systemic or ophthalmic) that may preclude safe administrationof the test article.

  • Use of contact lenses within 30 days of Visit 1.

  • Use of contact lenses during the study.

  • Participation in an investigational drug or device study within 30 days of enteringthis study.

  • Other protocol-defined exclusion criteria may apply.

Study Design

Total Participants: 726
Study Start date:
July 01, 2008
Estimated Completion Date:
May 31, 2009

Connect with a study center

  • Contact Alcon Call Center for Trial Locations

    Fort Worth, Texas 76134
    United States

    Site Not Available

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