NCT Number: NCT01242553
Clinical Validation Study for iVue
To demonstrate clinical substantial equivalence of iVue as comparable to commercially available RTVue.
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Observational
Primary location
Pacific Eye Specialists, Daly City, California, United States
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Normal: Normal results from clinical exam and free of ocular pathology.
- Glaucoma: Clinical exam results consistent with glaucoma and visual field defects consistent with glaucoma.
- Cornea: Clinical exam results consistent with cornea pathology.
- Retina: Clinical exam results consistent with retina pathology
Treatment and study plan
Primary outcomes
-
thickness of ocular structures
Sponsors and collaborators
Lead sponsor
Optovue
Industry
Registry information
Important dates
- Study start
- 2009
- Primary completion
- 2010
- Study completion
- 2010
- First posted
- Nov 17, 2010
- Registry last updated
- Sep 28, 2017
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.