A Study to Evaluate Retisert in the Treatment of Patients With the "Wet" Form of Age-Related Macular Degeneration

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2002 by Control Delivery Systems.
Recruitment status was  Active, not recruiting
Bausch & Lomb Incorporated
Information provided by:
Control Delivery Systems
ClinicalTrials.gov Identifier:
First received: March 20, 2002
Last updated: May 25, 2006
Last verified: December 2002
A study evaluating Retisert in patients with age-related macular degeneration

Condition Intervention Phase
Macular Degeneration
Drug: Retisert Implant
Phase 2

Study Type: Interventional
Study Design: Primary Purpose: Treatment

Resource links provided by NLM:

Further study details as provided by Control Delivery Systems:

Study Start Date: November 2001

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

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

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

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

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

ClinicalTrials.gov processed this record on May 26, 2016