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An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00329095
First Posted: May 24, 2006
Last Update Posted: May 24, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Robin, Alan L., M.D.
  Purpose
This is an open-label study in patients who are currently using either a topical prostaglandin as sole ocular hypotensive medical therapy q.d., or a topical prostaglandin plus an adjunctive topical ocular hypotensive marketed product either q.d., or b.i.d. in the same eye(s). Compliance will be measured over the two months of participation.

Condition Intervention Phase
Glaucoma Ocular Hypertension Drug: travoprost, latanoprost, or bimatoprost Drug: Additional ocular hypotensive medication Phase 4

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: An Evaluation of Use of Topical Ocular Hypotensive Medication by Electronic Compliance Measures

Resource links provided by NLM:


Further study details as provided by Robin, Alan L., M.D.:

Primary Outcome Measures:
  • Compliance.

Estimated Enrollment: 60
Study Start Date: December 2005
Estimated Study Completion Date: April 2006
Detailed Description:
This is an open-label study in patients who are currently using either a topical prostaglandin as sole ocular hypotensive medical therapy q.d., or a topical prostaglandin plus an adjunctive topical ocular hypotensive marketed product either q.d., or b.i.d. in the same eye(s). Compliance will be measured over the two months of participation.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Currently using one or two topical ocular hypotensive medications

Exclusion Criteria:

  • Hypersensitivity to any component of medication
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00329095


Sponsors and Collaborators
Robin, Alan L., M.D.
Investigators
Principal Investigator: Alan L. Robin, MD Alan L. Robin, M.D.
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00329095     History of Changes
Other Study ID Numbers: GMED-01
First Submitted: May 19, 2006
First Posted: May 24, 2006
Last Update Posted: May 24, 2006
Last Verified: May 2006

Keywords provided by Robin, Alan L., M.D.:
Glaucoma
Compliance

Additional relevant MeSH terms:
Glaucoma
Ocular Hypertension
Eye Diseases
Latanoprost
Bimatoprost
Travoprost
Antihypertensive Agents