- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01170481
Assessment of Retinal Nerve Fibre Layer by Optical Coherence Tomography in Uveitis Patients With Papilloedema
November 17, 2015 updated by: Carsten Heinz, St. Franziskus Hospital
Retinal Nerve Fibre Layer in Uveitic Secondary Glaucoma
Assessment of optic disc morphology can be difficult in patients with uveitis and papilloedema.
Therefore different optical coherence tomography (OCT) and laser scanning techniques may help to detect damage to the retinal nerve fibre layer.
Study Overview
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Muenster, Germany, 48145
- Department of Ophthalmology at St.-Franziskus Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 100 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
all patients with anterior or intermediate uveitis and papillooedema in fluoreszein angiography.
Description
Inclusion Criteria:
- anterior or intermediate uveitis
- papilloedema
- glaucoma
Exclusion Criteria:
- dense cataract
- dense vitreous opacification
- circular posterior synechiae
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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papilloedema without glaucoma
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papilloedema with glaucoma
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glaucoma without papilloedema
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Alterations of retinal nerve fibre layer by optical coherence tomography
Time Frame: once at study entry
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Baseline comparision of retinal nerve fibre layer thickness in patients with uveitis and with or without papilloedema at study entry.
No follow-up examination scheduled
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once at study entry
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Arnd Heiligenhaus, MD, Department at St. Franziskus Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2009
Primary Completion (Actual)
December 1, 2010
Study Completion (Actual)
April 1, 2011
Study Registration Dates
First Submitted
July 21, 2010
First Submitted That Met QC Criteria
July 26, 2010
First Posted (Estimate)
July 27, 2010
Study Record Updates
Last Update Posted (Estimate)
November 18, 2015
Last Update Submitted That Met QC Criteria
November 17, 2015
Last Verified
November 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2008-128-f-S
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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