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NCT00333463 Clinical Trial

Compliance With Once Daily Glaucoma Medication

Compliance Clinical Trial

Official title:
Compliance With Once Daily Glaucoma Medication

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00333463
Other study ID # CMS-06-03
Secondary ID
Status Completed
Phase N/A
First received June 1, 2006
Last updated November 17, 2016
Start date June 2006
Est. completion date September 2007

Study information
Verified date March 2010
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

A study to examine patient compliance with once daily glaucoma medication

Recruitment information / eligibility
Status Completed
Enrollment 700
Est. completion date September 2007
Est. primary completion date September 2007
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Primary open angle glaucoma or ocular hypertension patients

Exclusion Criteria:

Study Design

Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Behavioral:
• Intervention
The intervention group watched an educational video, reviewed current barriers to drop-taking and possible solutions with a study coordinator, received regular phone call reminders, and had audible and visible reminders activated on their DA devices.

Locations
Country Name City State
United States Ft. Worth Ft. Worth Texas

Sponsors (3)
Lead Sponsor Collaborator
Alcon Research Johns Hopkins University, University of Pennsylvania

Country where clinical trial is conducted

United States, 

References & Publications (1)

Okeke CO, Quigley HA, Jampel HD, Ying GS, Plyler RJ, Jiang Y, Friedman DS. Adherence with topical glaucoma medication monitored electronically the Travatan Dosing Aid study. Ophthalmology. 2009 Feb;116(2):191-9. doi: 10.1016/j.ophtha.2008.09.004. — View Citation

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