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A Study to Evaluate Retisert in the Treatment of Patients With the "Wet" Form of Age-Related Macular Degeneration
This study is ongoing, but not recruiting participants.
First Received: March 20, 2002   Last Updated: May 25, 2006   History of Changes
Sponsors and Collaborators: Control Delivery Systems
Bausch & Lomb, Inc.
Information provided by: Control Delivery Systems
ClinicalTrials.gov Identifier: NCT00032396
  Purpose

A study evaluating Retisert in patients with age-related macular degeneration


Condition Intervention Phase
Macular Degeneration
Drug: Retisert Implant
Phase II

Study Type: Interventional
Study Design: Treatment

Resource links provided by NLM:


Further study details as provided by Control Delivery Systems:

Study Start Date: November 2001
  Eligibility

Ages Eligible for Study:   55 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00032396

Locations
United States, Massachusetts
Control Delivery Systems, Inc.
Watertown, Massachusetts, United States, 02472
Sponsors and Collaborators
Control Delivery Systems
Bausch & Lomb, Inc.
  More Information

Additional Information:
No publications provided

Study ID Numbers: CDS FL-004
Study First Received: March 20, 2002
Last Updated: May 25, 2006
ClinicalTrials.gov Identifier: NCT00032396     History of Changes
Health Authority: United States: Food and Drug Administration

Keywords provided by Control Delivery Systems:
AMD
ARMD
Age-Related Macular Degeneration
Subfoveal Choroidal Neovascularization
CNV

Study placed in the following topic categories:
Fluocinolone Acetonide
Eye Diseases
Retinal Degeneration
Macular Degeneration
Neovascularization, Pathologic
Retinal Diseases
Choroidal Neovascularization

Additional relevant MeSH terms:
Eye Diseases
Retinal Degeneration
Macular Degeneration
Retinal Diseases

ClinicalTrials.gov processed this record on July 02, 2009