Acrylate Intraocular Lenses in Cataract Surgery of Uveitis Patients
NCT ID: NCT00403832
Last Updated: 2010-07-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2005-08-31
2007-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
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intraocular lenses: Two foldable, acrylic, sharp edged IOLs: AcrySof™ (AcrySof SA60AT, Alcon), and Akreos adapt™ (Bausch & Lomb)
Eligibility Criteria
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Inclusion Criteria
* no active inflammation
* significant visual disturbance related to lens opacification
Exclusion Criteria
* ocular hypertension/glaucoma
18 Years
ALL
No
Sponsors
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St. Franziskus Hospital
OTHER
Principal Investigators
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Arnd Heiligenhaus, Md Phd
Role: PRINCIPAL_INVESTIGATOR
Department of Ophthalmology at St.-FranziskusHospital Münster
Locations
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Department of Ophthalmology at St.-Franziskus Hospital
Münster, , Germany
Countries
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References
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Roesel M, Heinz C, Koch JM, Heiligenhaus A. Comparison of orbital floor triamcinolone acetonide and oral prednisolone for cataract surgery management in patients with non-infectious uveitis. Graefes Arch Clin Exp Ophthalmol. 2010 May;248(5):715-20. doi: 10.1007/s00417-009-1269-1. Epub 2010 Jan 16.
Related Links
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Related Info
Other Identifiers
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05-2911
Identifier Type: -
Identifier Source: org_study_id
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