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Sponsored by: |
Robin, Alan L., M.D. |
Information provided by: | Robin, Alan L., M.D. |
ClinicalTrials.gov Identifier: | NCT00329095 |
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 |
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 |
Estimated Enrollment: | 60 |
Study Start Date: | December 2005 |
Estimated Study Completion Date: | April 2006 |
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.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
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 |
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