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Macular Ganglion Cell Analysis (GCA) of the Cirrus HD-OCT in Glaucoma

C

Carl Zeiss Meditec

Status

Completed

Conditions

Glaucoma

Study type

Observational

Funder types

Industry

Identifiers

NCT01272102
HD-OCT-GCA-2010-1

Details and patient eligibility

About

To determine the area under the Receiver Operator Characteristic Curve (AUC) for the Ganglion Cell Analysis (GCA) average thickness.

Full description

To determine the area under the Receiver Operator Characteristic Curve (AUC) for the following GCA parameters:

  1. Minimum thickness
  2. Supero-temporal thickness
  3. Superior thickness
  4. Supero-nasal thickness
  5. Infero-temporal thickness
  6. Inferior thickness
  7. Infero-nasal thickness

Enrollment

119 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age of 40 years or older
  • Diagnosed to have glaucoma by the Principal Investigator or co-investigator
  • Able and willing to make the required study visits
  • Able and willing to give consent and follow study instructions

Exclusion criteria

Ophthalmic:

  • Best corrected visual acuity in either eye worse than 20/40 on a Snellen chart or on a Snellen equivalent acuity chart.
  • Refractive error outside -12.00D to +8.00D spherical range or >-3.00D cylinder.
  • Previous vitreoretinal surgery in study eye.
  • Vitreoretinal traction or epiretinal membrane in the study eye.
  • Any active infection of anterior or posterior segments.
  • Evidence of diabetic retinopathy, diabetic macular edema, or other vitreoretinal disease in the study eye upon dilated examination, or upon evaluation of retinal photos.

Systemic:

  • History of diabetes, leukemia, AIDS, uncontrolled systemic hypertension, dementia or multiple sclerosis.
  • A life threatening or debilitating disease.
  • Participation in any study involving a non-FDA approved investigational drug (IND) within the past month, or ongoing participation in a study with a non-FDA approved or cleared investigational device (IDE).
  • Current or recent (within the past 14 days) use of an agent with photosensitizing properties by any route (e.g., Visudyne®, ciprofloxacin, Bactrim®, doxycycline, etc.).
  • Concomitant use of hydrochloroquine and/or chloroquine.

Trial design

119 participants in 1 patient group

Glaucoma
Description:
subjects with glaucoma

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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