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Clinical Trials/NCT00798694
NCT00798694
Completed
Phase 4

Ocular Surface Changes With Topical Prostaglandin Analog Therapy

Wills Eye1 site in 1 country58 target enrollmentNovember 2008
ConditionsGlaucoma
InterventionsXalatanTravatan Z

Overview

Phase
Phase 4
Intervention
Xalatan
Conditions
Glaucoma
Sponsor
Wills Eye
Enrollment
58
Locations
1
Primary Endpoint
Change in Tear Break up Time (TBUT)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

To determine whether one glaucoma eye drop is less likely to cause changes to the surface of the eye (conjunctiva) than another. The two different prostaglandins are Xalatan and Travatan Z.

Detailed Description

Two groups will be entered into this study: group 1 will be naive to treatment and group 2 will be using Xalatan for at least one month before enrollment. Both groups will be using one drop at bedtime of Xalatan in the right eye and one drop at bedtime of Travatan Z in the left eye. Both of these drops are presently on the market and approved by the FDA for treatment of lowering eye pressure. Because this study will be masked, the examining clinician will not know what study drop each patient has been using.

Registry
clinicaltrials.gov
Start Date
November 2008
End Date
February 2011
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Wills Eye
Responsible Party
Principal Investigator
Principal Investigator

L. Jay Katz MD

Principal Investigator

Wills Eye

Eligibility Criteria

Inclusion Criteria

  • Age 21 or older
  • Able to understand protocol and agree to 3 visits
  • Any type of glaucoma
  • Selective laser trabeculoplasty, Argon laser trabeculoplasty, peripheral iridotomy accepted
  • Naïve: No prior glaucoma treatment (medical or surgical)
  • If patient non-compliant, must be off meds 3 months
  • Xalatan: At least one month use

Exclusion Criteria

  • Both Groups: Any history of ocular surface disease
  • Dry eye syndrome or prior Restasis use
  • Prior ocular surgery other than cataract extractions
  • Uveitis or other inflammatory disease of the eye or adnexa
  • Systemic medications that might influence ocular inflammation
  • Any active inflammation or infection
  • Pregnancy or intention to become pregnant
  • Naïve: Prior use of topical glaucoma medication unless off for 3 months.
  • Use of preserved artificial tear preparations in last 30 days and more than one year history of chronic use
  • Xalatan: Prior use of Travatan or Travatan Z

Arms & Interventions

New to Meds

Naive to glaucoma therapy medical or surgical. All patients will receive Xalatan in the right eye and Travatan Z in the left eye.

Intervention: Xalatan

New to Meds

Naive to glaucoma therapy medical or surgical. All patients will receive Xalatan in the right eye and Travatan Z in the left eye.

Intervention: Travatan Z

Currently on Xalatan

Patients currently on Xalatan at least one month. All patients will receive Xalatan in the right eye and Travatan Z in the left eye.

Intervention: Xalatan

Currently on Xalatan

Patients currently on Xalatan at least one month. All patients will receive Xalatan in the right eye and Travatan Z in the left eye.

Intervention: Travatan Z

Outcomes

Primary Outcomes

Change in Tear Break up Time (TBUT)

Time Frame: Baseline, 1 month, 2 months

Difference of tear break up time (in seconds, average of 3 measurements) at one and two months after enrollment.

Secondary Outcomes

  • Tear Production(Baseline, 1 month, 2 months)
  • Conjunctival Hyperemia Score(Baseline, 1 month, 2 months)
  • Intraocular Pressure(Baseline, 1 month, 2 months)
  • Ocular Surface Disease Index Score(Baseline, 1 month, 2 months)
  • Corneal Staining Score(Baseline, 1 month, 2 months)

Study Sites (1)

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