CDDR: Computer Detection of Diabetic Retinopathy Compared to Clinical Examination

Sponsor
IDx LLC (Industry)
Overall Status
Completed
CT.gov ID
NCT01625598
Collaborator
University of Pennsylvania (Other), University of Iowa (Other), The University of Texas Health Science Center, Houston (Other), Iowa Eye Center, Cedar Rapids IA (Other), VitreoRetinal Surgery, PA (Other), Retina Consultants Houston (Other), Barnet Dulaney Perkins Eye Center (Other)
600
7
24
85.7
3.6

Study Details

Study Description

Brief Summary

The hypothesis is that computer detection of the severity of diabetic retinopathy including the presence of clinically significant macular edema is not inferior to the detection using a dilated eye examination by a Board-certified ophthalmologist.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Photography of the retina
  • Procedure: Retinal photography

Detailed Description

The project is a multicenter, observational study to compare the accuracy of the IDX-DR computer detection system to board certified ophthalmologists performing dilated eye examination at identifying between no or mild NPDR without clinically significant diabetic macular edema from more than mild NPDR with or without CSDME. Approximately 400-600 persons with diabetes will be recruited through 5 clinical centers. The ophthalmologist who examines the patient will evaluate and record the status of the eye based on his/her clinical examination. The study subjects will then have two fundus photographs taken of each eye. The photographic images will be transferred to a central Reading Center at the University of Pennsylvania and interpreted by professional graders. The Reading Center will then transfer the images to IDx-DR, the computer detection system. IDx-LLC, the Sponsor of this study, will have no access to the images. Data from the Reading Center interpretation will be considered the "gold standard". The results of the clinical examination and IDX-DR will be compared against this gold standard as well as against each other.

Study Design

Study Type:
Observational
Actual Enrollment :
600 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
A Multicenter Masked Study to Compare Analysis of the Detection Program IDx-DR Against Standard of Care Clinical Examination by Ophthalmologists to Differentiate Levels of Diabetic Retinopathy and Diabetic Macular Edema
Study Start Date :
Apr 1, 2012
Actual Primary Completion Date :
Apr 1, 2014
Actual Study Completion Date :
Apr 1, 2014

Arms and Interventions

Arm Intervention/Treatment
People with diabetes

People with diabetes who are referred to an ophthalmologist for a dilated eye examination

Procedure: Photography of the retina
Every subject will undergo photography of the retina in both eyes

Procedure: Retinal photography
Device Subjects will have photography of both eyes

Outcome Measures

Primary Outcome Measures

  1. Sensitivity of detecting moderate non proliferative diabetic retinopathy or more severe DR and/or significant macular edema on a person-specific basis. [Recruitment over 4 months]

    If the interval excludes differences of 10% or more (IDx worse than clinical examination), then the IDx system will be considered non-inferior to clinical examination by ophthalmologists. If IDx is non-inferior to clinical examination, a two-sided test of the null hypothesis that the difference in sensitivities is 0 will be conducted to determine if the IDX is superior to clinical examination. 24 McNemar's test for paired proportions will be used to test the difference in proportions.

Secondary Outcome Measures

  1. Specificity (true negatives divided by true negatives plus false positives) at detecting more than moderate non proliferative diabetic retinopathy and/or significant macular edema on a person-specific basis. [Four months]

    Secondary Outcome Variables: Specificity on a person-specific basis Sensitivity on an eye-specific basis [Clinical examination only] Specificity on an eye-specific basis [Clinical examination only]

  2. Sensitivity on an eye-specific basis [Clinical examination only] [Four months]

    Analysis of secondary outcomes will follow the same approach as for the primary outcome analysis of paired proportions as described above for the comparison of person-specific sensitivity.

  3. Specificity on an eye-specific basis [Clinical examination only] [Four months]

    Analysis of secondary outcomes will follow the same approach as for the primary outcome for analysis of paired proportions as described above for the comparison of person-specific sensitivity.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • a diagnosis of diabetes mellitus

  • subject understands study and has signed informed consent

  • no history of any other retinal vascular disease, glaucoma, or other disease that may affect the appearance of the retina or optic disc (refractive error and ocular surface disease are allowed);

  • other than cataract surgery, no history of intraocular surgery, ocular laser treatments for any retinal disease, or ocular injections for diabetic macular edema or proliferative disease

  • no media opacity precluding good retinal photography

  • age 18 or older

Exclusion Criteria:
  • no diagnosis of diabetes mellitus

  • potential subject cannot understand study or informed consent

  • a history of retinal vascular disease other than due to diabetic retinopathy, glaucoma, or other disease that may affect the appearance of the retina or optic disc

  • previous intraocular surgery other than cataract; previous laser to the retina; or previous intraocular injections for the treatment of diabetic retinopathy

  • a media opacity in either eye that is severe enough to preclude good retinal photography

Contacts and Locations

Locations

Site City State Country Postal Code
1 Barnet Dulaney Perkins Eye Center Mesa Arizona United States 85206
2 Barnet Dulaney Perkins Eye Center Phoenix Arizona United States 85016
3 Iowa Eye Center Cedar Rapids Iowa United States 52403
4 University of Iowa Department of Ophthalmology and Visual Sciences Iowa City Iowa United States 52242
5 Retina Consultants of Houston Houston Texas United States 77030
6 Robert Cizik Eye Clinic - University of Texas Houston Houston Texas United States 77030
7 Retina Consultants of Houston Houston Texas United States 77090

Sponsors and Collaborators

  • IDx LLC
  • University of Pennsylvania
  • University of Iowa
  • The University of Texas Health Science Center, Houston
  • Iowa Eye Center, Cedar Rapids IA
  • VitreoRetinal Surgery, PA
  • Retina Consultants Houston
  • Barnet Dulaney Perkins Eye Center

Investigators

  • Principal Investigator: Jordan Graff, MD, Barnet Dulaney Perkins Eye Center - Phoenix & Mesa AZ
  • Principal Investigator: Brian Privett, MD, Iowa Eye Center, Cedar Rapids IA
  • Principal Investigator: Timothy Johnson, MD, University of Iowa, Iowa City IA
  • Principal Investigator: James Major, MD, Retina Consultants of Houston - Houston TX (2 locations)
  • Principal Investigator: Judianne Kellaway, MD, Robert Cizik Eye Center - University of Texas Houston

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
IDx LLC
ClinicalTrials.gov Identifier:
NCT01625598
Other Study ID Numbers:
  • 001
First Posted:
Jun 21, 2012
Last Update Posted:
Apr 22, 2014
Last Verified:
Apr 1, 2014

Study Results

No Results Posted as of Apr 22, 2014