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An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance

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ClinicalTrials.gov Identifier: NCT00329095
Recruitment Status : Completed
First Posted : May 24, 2006
Last Update Posted : May 24, 2006
Sponsor:
Information provided by:
Robin, Alan L., M.D.

Study Description
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Brief Summary:
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 or disease Intervention/treatment Phase
Glaucoma Ocular Hypertension Drug: travoprost, latanoprost, or bimatoprost Drug: Additional ocular hypotensive medication Phase 4

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.

Study Design
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Study Type : Interventional  (Clinical Trial)
Enrollment : 60 participants
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
Study Start Date : December 2005
Study Completion Date : April 2006

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U.S. FDA Resources

Arms and Interventions
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Outcome Measures
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Primary Outcome Measures :
  1. Compliance.

Eligibility Criteria
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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
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

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
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations 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 Posted: May 24, 2006    Key Record Dates
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