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A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Anterior Uveitis

Primary Purpose

Anterior Uveitis

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Dexamethasone
Sponsored by
Allergan
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anterior Uveitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 18 years or older with a diagnosis of non-infectious anterior uveitis in at least one eye Exclusion Criteria: Uncontrolled systemic disease Any active ocular infections

Sites / Locations

Outcomes

Primary Outcome Measures

Anterior Chamber Cell

Secondary Outcome Measures

Full Information

First Posted
June 2, 2006
Last Updated
May 27, 2011
Sponsor
Allergan
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1. Study Identification

Unique Protocol Identification Number
NCT00333996
Brief Title
A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Anterior Uveitis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2011
Overall Recruitment Status
Terminated
Study Start Date
May 2006 (undefined)
Primary Completion Date
March 2007 (Actual)
Study Completion Date
March 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Allergan

4. Oversight

5. Study Description

Brief Summary
This study will evaluate the safety and efficacy of an intravitreal implant of dexamethasone for the treatment of non-infectious anterior uveitis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Uveitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Primary Outcome Measure Information:
Title
Anterior Chamber Cell

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years or older with a diagnosis of non-infectious anterior uveitis in at least one eye Exclusion Criteria: Uncontrolled systemic disease Any active ocular infections
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Allergan Inc.
Organizational Affiliation
Allergan
Official's Role
Study Chair
Facility Information:
City
Dallas
State/Province
Texas
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Anterior Uveitis

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