Clinical trialNCT00133952CompletedPhase 3Interventional
Effect of Ruboxistaurin on Clinically Significant Macular Edema
SponsorChromaderm, Inc.Enrollment309Diabetic Macular Edema
Summary
The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →
Investigators
The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.
- Karl Beutner
Chromaderm, Inc.
Study Director
A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.
Sites
41 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.
Canada
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Halifax, Nova Scotia, Canada
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London, Ontario, Canada
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Mississauga, Ontario, Canada
Denmark
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Aarhus, Denmark
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Glostrup Municipality, Denmark
Germany
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Bonn, Germany
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Leipzig, Germany
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Münster, Germany
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Ulm, Germany
Lithuania
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Kaunas, Lithuania
Mexico
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Mexico City, Mexico
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Monterrey, Mexico
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San Luis Potosí City, Mexico
Portugal
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Coimbra, Portugal
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Lisbon, Portugal
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Porto, Portugal
Romania
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Bucharest, Romania
Spain
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Alicante, Spain
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Barcelona, Spain
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Valladolid, Spain
United Kingdom
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London, Greater London, United Kingdom
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London, United Kingdom
United States
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Phoenix, Arizona, United States
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Artesia, California, United States
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Newark, Delaware, United States
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Jacksonville, Florida, United States
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Augusta, Georgia, United States
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Indianapolis, Indiana, United States
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Baltimore, Maryland, United States
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Boston, Massachusetts, United States
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Grand Rapids, Michigan, United States
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Portsmouth, New Hampshire, United States
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Slingerlands, New York, United States
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Asheville, North Carolina, United States
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Lakewood, Ohio, United States
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Kingston, Pennsylvania, United States
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Pittsburgh, Pennsylvania, United States
- for Additional Information Regarding Investigative Sites for This Trial, Contact 1-877-Ctlilly (1-877-285-4559, 1-317-615-4559) Mon - Fri From 9 Am To 5 Pm Eastern Time (utc/gmt - 5 Hours, Est), Or Speak With Your Personal Physician.
West Mifflin, Pennsylvania, United States
- for Additional Information Regarding Investigative Sites for This Trial, Contact 1-877-Ctlilly (1-877-285-4559, 1-317-615-4559) Mon - Fri From 9 Am To 5 Pm Eastern Time (utc/gmt - 5 Hours, Est), Or Speak With Your Personal Physician.
Dallas, Texas, United States
- for Additional Information Regarding Investigative Sites for This Trial, Contact 1-877-Ctlilly (1-877-285-4559, 1-317-615-4559) Mon - Fri From 9 Am To 5 Pm Eastern Time (utc/gmt - 5 Hours, Est), Or Speak With Your Personal Physician.
Houston, Texas, United States
Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.
Drugs studied
No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →
Registration & key dates
Registry attributes as recorded on the ClinicalTrials.gov study record.
- Start
- 31 Aug 2005
- Primary completion
- 31 Jul 2011
- Completion
- 31 Jul 2011
- Last update posted
- 6 Oct 2016
- Registered enrollment
- 309
- Registry id
- NCT00133952
Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.