An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance

This study has been completed.
Sponsor:
Information provided by:
Robin, Alan L., M.D.
ClinicalTrials.gov Identifier:
NCT00329095
First received: May 19, 2006
Last updated: May 22, 2006
Last verified: May 2006

May 19, 2006
May 22, 2006
December 2005
Not Provided
Compliance.
Same as current
Complete list of historical versions of study NCT00329095 on ClinicalTrials.gov Archive Site
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An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance
An Evaluation of Use of Topical Ocular Hypotensive Medication by Electronic Compliance Measures

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.

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.

Interventional
Phase 4
Allocation: Non-Randomized
Endpoint Classification: Pharmacodynamics Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Diagnostic
  • Glaucoma
  • Ocular Hypertension
  • Drug: travoprost, latanoprost, or bimatoprost
  • Drug: Additional ocular hypotensive medication
Not Provided
Robin AL, Novack GD, Covert DW, Crockett RS, Marcic TS. Adherence in glaucoma: objective measurements of once-daily and adjunctive medication use. Am J Ophthalmol. 2007 Oct;144(4):533-40. Epub 2007 Aug 8.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
60
April 2006
Not Provided

Inclusion Criteria:

  • Currently using one or two topical ocular hypotensive medications

Exclusion Criteria:

  • Hypersensitivity to any component of medication
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT00329095
GMED-01
Not Provided
Not Provided
Robin, Alan L., M.D.
Not Provided
Principal Investigator: Alan L. Robin, MD Alan L. Robin, M.D.
Robin, Alan L., M.D.
May 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP