Clinical Trials Directory

Trials / Completed

CompletedNCT02138461

Tolerability of Bimatoprost 0.01% vs Latanoprost Eye Drops

Subjective Patient Assessment Comparing Overall Tolerability and Satisfaction of a Prostaglandin Analogue Including Either Bimatoprost 0.01% or Latanoprost.

Status
Completed
Phase
Study type
Observational
Enrollment
211 (actual)
Sponsor
MDbackline, LLC · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study examines patient perceptions regarding the tolerability of two classes of glaucoma medication: bimatoprost and latanoprost.

Detailed description

Patients enrolled in this study completed a validated survey instrument (COMTOL) examining tolerability of topically applied ophthalmic medications that they are already taking in their regular course of care for glaucoma. The purpose of the study is to determine whether side effects and symptoms of the drugs already being taken cause problems with activities of daily living.

Conditions

Timeline

Start date
2013-10-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2014-05-14
Last updated
2014-09-25
Results posted
2014-09-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02138461. Inclusion in this directory is not an endorsement.

Tolerability of Bimatoprost 0.01% vs Latanoprost Eye Drops (NCT02138461) · Clinical Trials Directory