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Stratus Versus Cirrus OCT in AMD
This study is currently recruiting participants.
Verified by The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery, December 2007
Sponsored by: The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery
Information provided by: The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery
ClinicalTrials.gov Identifier: NCT00568191
  Purpose

The Cirrus OCT provides due to the spectral domain technology a 2-fold resolution than Stratus OCT generated in a comparable amount of time. Due to this higher resolution the retinal surface and the retinal pigment epithelium can be identified more clearly, a significantly reduced number of algorithm failures is expected


Condition
Age-Related Macular Degeneration
Choroidal Neovascularization

Genetics Home Reference related topics: X-linked juvenile retinoschisis
MedlinePlus related topics: Macular Degeneration
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Reliability of Threshold Algorithm in Age-Related Macular Degeneration: Stratus Versus Cirrus OCT

Further study details as provided by The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery:

Primary Outcome Measures:
  • Number of algorithm failures assessed by Stratus OCT versus Cirrus OCT in the horizontal central line [ Time Frame: only 1 examination ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Number of algorrithm failures in Stratus versus Cirrus OCT assessed in the whole scan [ Time Frame: 1 examination ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 100
Study Start Date: October 2007
Estimated Study Completion Date: December 2007
Groups/Cohorts
1
retinal thickness program Stratus OCT software 4.0
2
retinal cube 200x200 program of Cirrus OCT

  Eligibility

Ages Eligible for Study:   55 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients aged > 55 years of either sex presenting with age-related macular degeneration

Criteria

Inclusion Criteria:

  • Age>55 years
  • Age-related macular degeneration

Exclusion Criteria:

  • Not consented patients
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00568191

Contacts
Contact: Ilse Krebs, MD +43171165 ext 94607 Ilse.Krebs@wienkav.at

Locations
Austria
Ludwig Boltzmann Institute for Retinology and Biomicroscopic Lasersurgery Recruiting
Vienna, Austria, A1030
Contact: Ilse Krebs, MD     +43171165 ext 4607     Ilse.Krebs@wienkav.at    
Principal Investigator: Ilse Krebs, MD            
Sponsors and Collaborators
The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery
Investigators
Principal Investigator: Ilse Krebs Ludwig Boltzmann Institute of Retinology and Biomicroscopic Lasersurgery
  More Information

Responsible Party: The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery ( Prof Susanne Binder )
Study ID Numbers: EK 06-007-VK1
Study First Received: December 4, 2007
Last Updated: December 4, 2007
ClinicalTrials.gov Identifier: NCT00568191  
Health Authority: Austria: Ethikkommission

Keywords provided by The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery:
Age-related macular degeneration
choroidal neovascularization
Stratus OCT
Cirrus OCT

Study placed in the following topic categories:
Metaplasia
Eye Diseases
Choroid Diseases
Retinal Degeneration
Macular Degeneration
Neovascularization, Pathologic
Retinal Diseases
Retinal degeneration
Choroidal Neovascularization

Additional relevant MeSH terms:
Uveal Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on January 15, 2009