Wheaton, Illinois, United States
NCT Number: NCT02348476
A Study of Simbrinza™ Therapy in Patients With Open-Angle Glaucoma or Ocular Hypertension
This study is a retrospective chart review to assess the tolerability and efficacy of treatment with Simbrinza™ used for patients with Open-Angle Glaucoma or Ocular Hypertension.
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Notify MeKey information
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Participants treated with Simbrinza™ for Intra-Ocular Pressure (IOP) lowering in at least one eye
- Participants who had at least one-follow-up visit with tolerablity and efficacy data after Simbrinza™ treatment initiation.
Exclusion criteria
- Active ocular disease other than glaucoma or ocular hypertension
- History of any intraocular surgery or glaucoma laser surgery within 3 months.
Treatment and study plan
No intervention
OtherNo study drug is administered in this study.
Primary outcomes
-
The time to first glaucoma therapy escalation occurrence or discontinuation of Simbrinza®
Time frame: 2 Years
Secondary outcomes
-
The time to first glaucoma therapy escalation occurrence
Time frame: 2 Years
-
The time(s) to additional glaucoma therapy escalation occurrence(s)
Time frame: 2 Years
-
Specific AEs and SAEs occurring with a frequency of ≥5%
Time frame: 2 Years
Sponsors and collaborators
Lead sponsor
Allergan
Industry
Registry information
Important dates
- Study start
- 2014
- Primary completion
- 2015
- Study completion
- 2015
- First posted
- Jan 28, 2015
- Registry last updated
- Sep 21, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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