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
PHASE4
24 participants
INTERVENTIONAL
2005-12-31
2007-05-31
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
DOUBLE
Study Groups
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A
cataract surgery (Hoya AF-1 [UY] YA-60BB)
implantation of a yellow Hoya AF-1 (UY) YA-60BB intraocular lens
B
cataract surgery (Hoya AF-1 [UV] VA-60BB lens)
implantation of an uncoloured Hoya AF-1 (UV) VA-60BB
Interventions
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cataract surgery (Hoya AF-1 [UY] YA-60BB)
implantation of a yellow Hoya AF-1 (UY) YA-60BB intraocular lens
cataract surgery (Hoya AF-1 [UV] VA-60BB lens)
implantation of an uncoloured Hoya AF-1 (UV) VA-60BB
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* age 55 to 80 years
* expected postoperative visual acuity of at least 1.0
Exclusion Criteria
* corneal scars
* diabetes
* arterial hypertonia
* pseudoexfoliation-syndrome
* earlier ocular surgeries or laser treatments
* intraocular tumors
* color abnormalities
* expected postoperative visual acuity lower 1.0
55 Years
80 Years
ALL
No
Sponsors
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Hospital Hietzing
OTHER
Responsible Party
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Dept. of Ophthalmology, Hospital Hietzing, Vienna, Austria
Principal Investigators
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Matthias G Wirtitsch, MD
Role: PRINCIPAL_INVESTIGATOR
Dept of Ophthalmology, Hietzing Hospital, Vienna, Austria
Locations
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Department of Ophthalmology, Hietzing Hospital
Vienna, , Austria
Countries
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Other Identifiers
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Ye-Whi 2006
Identifier Type: -
Identifier Source: org_study_id
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