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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01284478
Other study ID # NCRVA-2011-Ozurdex-16-1
Secondary ID
Status Completed
Phase Phase 2
First received January 25, 2011
Last updated October 3, 2012
Start date January 2011
Est. completion date October 2012

Study information

Verified date October 2012
Source Northern California Retina Vitreous Associates
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to determine where a sustained steroid delivery system (Ozurdex,Allergan) is safe and effective to treat Cystoid Macular Edema in diabetic patients after Cataract Surgery


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date October 2012
Est. primary completion date October 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- DIABETIC PATIENTS WHO DEVELOP CYSTOID MACULA EDEMA AFTER CATARACT SURGERY (WITHIN 4-10 WEEKS AFTER SURGERY

- VISUAL ACUITY WORSE THAN 20/32

Exclusion Criteria:

- VISUAL ACUITY WORSE THAN 20/200

- MODERATE OR SEVERE GLAUCOMA (AS DEFINED AS USING >2 TOPICAL GLAUCOMA MEDIATIONS.

- USE OF SYSTEMIC, PERIOCULAR OR INTRAOCULAR CORTICOSTEROIDS WITHIN 30 DAYS OF ENROLLMENT

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dexamethasone Implant
Ozurdex (Dexamethasone Implant), 0.7 mg will injected intravitreally

Locations

Country Name City State
United States Northern California Retina Vitreous Associates Mountain View California

Sponsors (2)

Lead Sponsor Collaborator
Northern California Retina Vitreous Associates Allergan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary BEST CORRECTED VISUAL ACUITY (ETDRS) AT DAY 180
Secondary RETINAL THICKNESS MEASURED BY SPECTRAL DOMAIN OPTICAL TOMOGRAPHY CENTRAL FOVEAL THICKNESS AND MACULAR VOULUME 90 and 180 DAYS
See also
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Terminated NCT04603937 - A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME) Phase 3
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