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A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulting From Branch Retinal Vein Occlusion

Primary Purpose

Macular Degeneration, Macular Edema, Branch Retinal Vein Occlusion

Status
Completed
Phase
Phase 1
Locations
Japan
Study Type
Interventional
Intervention
dexamethasone
Sponsored by
Sanwa Kagaku Kenkyusho Co., Ltd.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Macular Degeneration focused on measuring eye diseases

Eligibility Criteria

20 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Macular edema resulting from branch retinal vein condition The criteria for visual acuity and macular thickness are met Exclusion Criteria: History of glaucoma Diabetic retinopathy Known steroid-responder Use of systemic steroids Use of Warfarin/Heparin

Sites / Locations

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
March 27, 2006
Last Updated
February 9, 2012
Sponsor
Sanwa Kagaku Kenkyusho Co., Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT00308477
Brief Title
A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulting From Branch Retinal Vein Occlusion
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators

Name of the Sponsor
Sanwa Kagaku Kenkyusho Co., Ltd.

4. Oversight

5. Study Description

Brief Summary
This study will evaluate the safety and efficacy of the intravitreal implant of dexamethasone for the treatment of macular edema associated with branch retinal vein occlusion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Macular Degeneration, Macular Edema, Branch Retinal Vein Occlusion
Keywords
eye diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
dexamethasone

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Macular edema resulting from branch retinal vein condition The criteria for visual acuity and macular thickness are met Exclusion Criteria: History of glaucoma Diabetic retinopathy Known steroid-responder Use of systemic steroids Use of Warfarin/Heparin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clinical Study Group, Clinical Development Dept.
Organizational Affiliation
Sanwa Kagaku Kenkyusho Co., Ltd.
Official's Role
Study Director
Facility Information:
City
Aichi
Country
Japan
City
Chiba
Country
Japan
City
Fukuoka
Country
Japan
City
Gunma
Country
Japan
City
Hokkaido
Country
Japan
City
Kagawa
Country
Japan
City
Kyoto
Country
Japan
City
Mie
Country
Japan
City
Miyazaki
Country
Japan
City
Osaka
Country
Japan
City
Shiga
Country
Japan
City
Tokyo
Country
Japan

12. IPD Sharing Statement

Learn more about this trial

A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulting From Branch Retinal Vein Occlusion

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