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An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance

This study has been completed.

Sponsored by: Robin, Alan L., M.D.
Information provided by: Robin, Alan L., M.D.
ClinicalTrials.gov Identifier: NCT00329095
  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 IV

Genetics Home Reference related topics:   early-onset glaucoma   

MedlinePlus related topics:   Glaucoma    High Blood Pressure   

ChemIDplus related topics:   Latanoprost    Travoprost    Bimatoprost   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Diagnostic, Non-Randomized, Open Label, Uncontrolled, Parallel Assignment, Pharmacodynamics Study
Official Title:   An Evaluation of Use of Topical Ocular Hypotensive Medication by Electronic Compliance Measures

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
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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

Please refer to this study by its ClinicalTrials.gov identifier: NCT00329095

Sponsors and Collaborators
Robin, Alan L., M.D.

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


Publications indexed to this study:

Study ID Numbers:   GMED-01
First Received:   May 19, 2006
Last Updated:   May 22, 2006
ClinicalTrials.gov Identifier:   NCT00329095
Health Authority:   United States: Institutional Review Board

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

Study placed in the following topic categories:
Bimatoprost
Glaucoma
Eye Diseases
Vascular Diseases
Latanoprost
Travoprost
Hypertension
Ocular Hypertension

Additional relevant MeSH terms:
Therapeutic Uses
Cardiovascular Diseases
Cardiovascular Agents
Antihypertensive Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 07, 2008




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