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Compliance With Once Daily Glaucoma Medication

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00333463
First Posted: June 5, 2006
Last Update Posted: November 18, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
Johns Hopkins University
University of Pennsylvania
Information provided by (Responsible Party):
Alcon Research
June 1, 2006
June 5, 2006
November 18, 2016
June 2006
September 2007   (Final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00333463 on ClinicalTrials.gov Archive Site
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Compliance With Once Daily Glaucoma Medication
Compliance With Once Daily Glaucoma Medication
A study to examine patient compliance with once daily glaucoma medication
Not Provided
Observational
Time Perspective: Retrospective
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Probability Sample
Primary open angle glaucoma or ocular hypertension patients
Compliance
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.
  • Intervention group
    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.
    Intervention: Behavioral: Intervention
  • Non-Intervention Group
    The control group was told to take drops as prescribed and received no additional intervention.
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. Epub 2008 Dec 12.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
700
September 2007
September 2007   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Primary open angle glaucoma or ocular hypertension patients

Exclusion Criteria:

Sexes Eligible for Study: All
Child, Adult, Senior
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00333463
CMS-06-03
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Alcon Research
Alcon Research
  • Johns Hopkins University
  • University of Pennsylvania
Study Director: David Friedman, MD Study Director
Alcon Research
March 2010