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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00564291
Other study ID # KEK 044/07
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2007
Est. completion date November 28, 2023

Study information

Verified date November 2023
Source Insel Gruppe AG, University Hospital Bern
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Comparison of different OCT instruments to assess retinal thickness, correlation to fluorescein angiography, and visual outcome after therapy with anti-VEGF therapy


Description:

Comparison of different OCT instruments to assess retinal thickness, correlation to fluorescein angiography, and visual outcome after therapy with anti-VEGF therapy


Recruitment information / eligibility

Status Completed
Enrollment 700
Est. completion date November 28, 2023
Est. primary completion date November 27, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Macular disease - Healthy subjects

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Examination with an OCT device


Locations

Country Name City State
Switzerland Dep. Ophthalmology, University Hospital Bern Bern
Switzerland Klinik und Poliklinik für Augenheilkunde, University Bern Bern

Sponsors (2)

Lead Sponsor Collaborator
Sebastian Wolf University of Bern

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Integrity of retinal layers End of study
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