An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance
1 other identifier
interventional
60
0 countries
N/A
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_4
Started Dec 2005
Shorter than P25 for phase_4
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2006
CompletedFirst Submitted
Initial submission to the registry
May 19, 2006
CompletedFirst Posted
Study publicly available on registry
May 24, 2006
CompletedMay 24, 2006
May 1, 2006
May 19, 2006
May 22, 2006
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Compliance.
Interventions
Eligibility Criteria
You may qualify if:
- Currently using one or two topical ocular hypotensive medications
You may not qualify if:
- Hypersensitivity to any component of medication
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
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. doi: 10.1016/j.ajo.2007.06.012. Epub 2007 Aug 8.
PMID: 17686450DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Alan L. Robin, MD
Alan L. Robin, M.D.
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- PARALLEL
- Sponsor Type
- INDIV
Study Record Dates
First Submitted
May 19, 2006
First Posted
May 24, 2006
Study Start
December 1, 2005
Study Completion
April 1, 2006
Last Updated
May 24, 2006
Record last verified: 2006-05