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CompletedNCT01370850Updated Jun 10, 2011

Clinical Validation Study of RTVue Features

An observational study in Healthy and Glaucoma, sponsored by Optovue. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-06-10.

Sponsored by Optovue · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
53
Ages
18 Years and older
Sex
All
01

Study summary

To perform a clinical validation study of RTVue features in volunteers with various ocular pathology or no ocular pathology.

Read the detailed description

Clinical validation study of RTVue features in volunteers with various ocular pathology or no ocular pathology. Subjects to undergo a clinical exam and OCT scanning.

02

Conditions studied

  • Healthy
  • Glaucoma

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Keywords

  • Retina pathology
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 53 is below the median of 103 across 454 observational studies indexed under Glaucoma.

Browse Glaucoma studies →

Lead sponsor

Optovue is the lead sponsor of 16 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Volunteers with various ocular pathology or no ocular pathology

Inclusion criteria

  • Normal subjects will have normal results from the clinical exam and be free of ocular pathology.
  • Glaucoma patients will have clinical exam results consistent with glaucoma; they will have visual field defects consistent with glaucoma and/or structural damage consistent with glaucoma.
  • Retina patients will have clinical exam results consistent with retina pathology.

Exclusion criteria

Exclusion Criteria:

  • Normal subjects will be free of any ocular pathology.
  • Glaucoma patients will be free of any ocular pathology except glaucoma.
  • Retina patients will be free of any ocular pathology except any type of retina pathology.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
53 participants (actual)

Groups and cohorts

  • Normal

    Normal results from the clinical exam and free of ocular pathology.

  • Glaucoma

    Clinical exam results consistent with glaucoma; visual field defects consistent with glaucoma and/or structural damage consistent with glaucoma.

  • Retina

    Clinical exam results consistent with retina pathology.

06

What researchers measure

Primary outcomes

  1. Retina measurement

    Time frame: at time of study visit (day 1)

07

Study locations

1 site
  • Pacific Eye Specialists
    Daly City, California 94015, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 10, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01370850
Lead sponsor
Optovue
First posted
Jun 10, 2011
Start date
Mar 2011
Primary completion
Apr 2011
Completion
Apr 2011
Last update
Jun 10, 2011

Study contacts

Mike Sinai, PhD
study director · Optovue

Oversight

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

Not currently enrolling

This study is completed, as verified in Jun 2011. You cannot join it, but the record below documents what was studied.

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