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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01512901
Other study ID # 01021104
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received January 15, 2012
Last updated July 17, 2014

Study information

Verified date July 2014
Source Santen Pharmaceutical Co., Ltd.
Contact n/a
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

This study will evaluate the efficacy and safety of Betamethasone Microsphere (DE-102) for macular edema following branch retinal vein occlusion


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- 20 years of age or older

- Diagnosis of macular edema following branch retinal vein occlusion

Exclusion Criteria:

- BCVA ETDRS letter score in non-study eye < 35

- Known steroid-responder

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Drug:
Betamethasone Microsphere (DE-102) Low Dose

Betamethasone Microsphere (DE-102) High Dose

Sham


Locations

Country Name City State
Japan Santen study sites Osaka
Korea, Republic of Santen study sites Seoul

Sponsors (1)

Lead Sponsor Collaborator
Santen Pharmaceutical Co., Ltd.

Countries where clinical trial is conducted

Japan,  Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline of Best Corrected Visual Acuity(BCVA) in ETDRS letter score
Secondary Change in retinal thickness from baseline