An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance

Sponsor
Robin, Alan L., M.D. (Other)
Overall Status
Completed
CT.gov ID
NCT00329095
Collaborator
(none)
60
4

Study Details

Study Description

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
  • 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

Study Type:
Interventional
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 :
Dec 1, 2005
Study Completion Date :
Apr 1, 2006

Outcome Measures

Primary Outcome Measures

  1. Compliance. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Currently using one or two topical ocular hypotensive medications
Exclusion Criteria:
  • Hypersensitivity to any component of medication

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Robin, Alan L., M.D.

Investigators

  • Principal Investigator: Alan L. Robin, MD, Alan L. Robin, M.D.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00329095
Other Study ID Numbers:
  • GMED-01
First Posted:
May 24, 2006
Last Update Posted:
May 24, 2006
Last Verified:
May 1, 2006

Study Results

No Results Posted as of May 24, 2006