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CompletedNCT00362622Updated Aug 16, 2012

Determinants of Compliance With Glaucoma Therapy

An observational study in Open Angle Glaucoma, sponsored by University of Alabama at Birmingham. Completed at 1 site in United States. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2012-08-16.

Sponsored by University of Alabama at Birmingham · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
59
Ages
19 Years and older
Sex
All
01

Study summary

To determine the association between medical, demographic, socioeconomic, and therapeutic differences on compliance with topical glaucoma therapy using the Travalert device.

Read the detailed description

To determine the association between medical, demographic, socioeconomic, and therapeutic differences on compliance with topical glaucoma therapy using the Travalert device. All participants will have open angle glaucoma.

02

Conditions studied

  • Open Angle Glaucoma

Keywords

  • Travalert
  • open angle glaucoma
03

In context

Glaucoma

1,818 studies on the registry are indexed under Glaucoma; 231 are open to participants now.

This study's enrollment of 59 is below the median of 103 across 454 observational studies indexed under Glaucoma.

Browse Glaucoma studies →

Lead sponsor

University of Alabama at Birmingham is the lead sponsor of 1,396 studies on the registry; 284 are open to participants now.

Of its 156 completed or terminated interventional studies of FDA-regulated products, 124 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Glaucoma patients.

Eligibility criteria

To be eligible to participate in the study, patients had to be (1) 19 years or older; (2) have a diagnosis of open angle glaucoma (OAG) in 1 or both eyes or ocular hypertension; and (3) using a prostaglandin ocular hypotensive medication in 1 or both eyes.

The protocol excluded patients with uncontrolled IOP control, known contraindications to Travoprost, clinically significant systemic disease that would interfere with the study, participation in any other research study within 30 days, or change in systemic medications that may alter IOP within 30 days before recruitment.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
59 participants (actual)
06

Study locations

1 site
  • University of Alabama at Birmingham
    Birmingham, Alabama 35294, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 16, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00362622
Lead sponsor
University of Alabama at Birmingham
Collaborators
Alcon Research
Responsible party
Christopher Girkin, MD (Chairman/Professor, University of Alabama at Birmingham) — Principal investigator
First posted
Aug 10, 2006
Start date
Oct 2005
Completion
Jan 2008
Last update
Aug 16, 2012

Study contacts

Christopher A Girkin, MD
principal investigator · University of Alabama at Birmingham
Jason Swanner, MD
principal investigator · University of Alabama at Birmingham
Matthew Sapp, MD
principal investigator · University of Alabama at Birmingham

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2012. You cannot join it, but the record below documents what was studied.

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