Retinal Thickness and Volume Estimates Given by Time Domain and Spectral Optical Coherence Tomography

Sponsor
Glostrup University Hospital, Copenhagen (Other)
Overall Status
Completed
CT.gov ID
NCT00873106
Collaborator
(none)
20
1
12.9
1.5

Study Details

Study Description

Brief Summary

The purpose of the present study is to determine if the retinal thickness estimates of the Stratus OCT, the 3D OCT-1000, and the CirrusHD OCT are comparable in diabetic and in healthy individuals (OCT=Optical Coherence Tomography).

Condition or Disease Intervention/Treatment Phase
  • Device: Optical coherence tomography

Study Design

Study Type:
Observational
Actual Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Retinal Thickness and Volume Estimates Given by Time Domain and Spectral Optical Coherence Tomography
Study Start Date :
Feb 1, 2009
Actual Primary Completion Date :
Mar 1, 2010
Actual Study Completion Date :
Mar 1, 2010

Outcome Measures

Primary Outcome Measures

  1. Retinal thickness and retinal volume from each OCT scan [within 24 hours]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • diabetic retinopathy in the diabetic group

  • healthy retinas in the healthy group

Exclusion Criteria:
  • not able to cooperate

  • retinal disease other than macular oedema

  • severe media opacities (e.g. cataract)

  • prior macular laser photocoagulation except for large oedemas

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Nordre Ringvej 57 Glostrup Copenhagen Denmark DK-2600

Sponsors and Collaborators

  • Glostrup University Hospital, Copenhagen

Investigators

  • Principal Investigator: Dorte Nellemann Thornit, MD, Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Nordre Ringvej 57, DK-2600 Glostrup, Denmark

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Birgit Sander, ph.d, Glostrup University Hospital, Copenhagen
ClinicalTrials.gov Identifier:
NCT00873106
Other Study ID Numbers:
  • OCT comparison
First Posted:
Apr 1, 2009
Last Update Posted:
Sep 6, 2012
Last Verified:
Sep 1, 2012
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 6, 2012