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CompletedNCT00873106Updated Sep 6, 2012

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

An observational study in Healthy and Diabetic Maculopathy, sponsored by Glostrup University Hospital, Copenhagen. Completed at 1 site in Denmark. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-09-06.

Sponsored by Glostrup University Hospital, Copenhagen · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
20
Ages
18 Years and older
Sex
All
01

Study 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).

02

Conditions studied

  • Healthy
  • Diabetic Maculopathy
03

In context

Macular Degeneration

1,474 studies on the registry are indexed under Macular Degeneration; 206 are open to participants now.

This study's enrollment of 20 is below the median of 106 across 421 observational studies indexed under Macular Degeneration.

Browse Macular Degeneration studies →

Lead sponsor

Glostrup University Hospital, Copenhagen is the lead sponsor of 104 studies on the registry; 5 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

A group of diabetic and healthy participants

Inclusion criteria

  • diabetic retinopathy in the diabetic group
  • healthy retinas in the healthy group

Exclusion criteria

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
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
20 participants (actual)

Interventions

  • DeviceOptical coherence tomography

    Stratus OCT: fast radial lines 3D OCT-1000: radial 2048 and 3D OCT Cirrus HD OCT: 3D OCT

06

What researchers measure

Primary outcomes

  1. Retinal thickness and retinal volume from each OCT scan

    Time frame: within 24 hours

07

Study locations

1 site
  • Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Nordre Ringvej 57
    Glostrup, Copenhagen DK-2600, Denmark
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 6, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00873106
Lead sponsor
Glostrup University Hospital, Copenhagen
Responsible party
Birgit Sander (ph.d, Glostrup University Hospital, Copenhagen) — Principal investigator
First posted
Apr 1, 2009
Start date
Feb 2009
Primary completion
Mar 2010
Completion
Mar 2010
Last update
Sep 6, 2012

Study contacts

Dorte Nellemann Thornit, MD
principal investigator · Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Nordre Ringvej 57, DK-2600 Glostrup, Denmark

Oversight

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

Not currently enrolling

This study is completed, as verified in Sep 2012. You cannot join it, but the record below documents what was studied.

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