Diabetic Macular Edema Clinical Trial
Official title:
Phase 2 Study of the Safety and Bioactivity of Topical Ocular Mecamylamine for the Treatment of Diabetic Macular Edema (DME)
| Verified date | April 2008 |
| Source | CoMentis |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This is an open-label study evaluating the safety and tolerability of topical ocular mecamylamine given twice a day in patients with diabetic macular edema (DME). Patients will be treated for 12 weeks.
| Status | Completed |
| Enrollment | 0 |
| Est. completion date | April 2008 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - macular edema due to diabetic retinopathy Exclusion Criteria: - vision loss from other ocular disease - intraocular surgery within 3 months - intraocular anti-VEGF or steroids within 3 months - HbA1c >12 |
| Country | Name | City | State |
|---|---|---|---|
| United States | Johns Hopkins School of Medicine / Wilmer Eye Institute | Baltimore | Maryland |
| United States | Ophthalmic Consultants of Boston | Boston | Massachusetts |
| United States | East Bay Retina Consultants, Inc. | Oakland | California |
| Lead Sponsor | Collaborator |
|---|---|
| CoMentis | Juvenile Diabetes Research Foundation |
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