Evaluation of the Effects of Selective Photocoagulation for the Treatment of Diabetic Macular Edema

Inclusion Criteria: 1. Best corrected ETDRS visual acuity letter score \>=24 (app. 20/320 or better) 2. Definite retinal thickness due to diabetic macular edema by on clinical exam at or within 500 to 3000 microns of the macular center (radius) for which the investigator believes laser photocoagulation is not indicated 3. A thickness equal or less than 315 microns in the central subfield (confirmed by SD-OCT). 4. A thickness of \>2 SD of norm in one or more inner or outer subfields on SD-OCT. 5. Maximal focal/grid laser not yet applied (within areas of thickening between 500 and 3000 microns from center of macula, not all microaneurysms treated with direct laser and not all other areas of thickening treated with grid laser). Maximal or complete laser treatment is defined as direct treatment to all microaneurysms within areas of edema and grid treatment to all other areas of macular edema. 6. No panretinal scatter photocoagulation (PRP) within prior 4 months. 7. No recent medical treatment for DME (e.g., intravitreal/peribulbar steroids within past 4 months or intravitreal anti-VEGF injection within past 2 months). 8. No major ocular surgery (including cataract extraction, any other intraocular surgery, scleral buckle, glaucoma filter, cornea transplant, etc.) within prior 6 months. 9. No Nd:YAG laser capsulotomy within prior 2 months. 10. Macular edema is not considered to be due to a cause other than diabetic macular edema o An eye should not be considered eligible (1) if the macular edema is considered to be related to cataract extraction or (2) clinical exam and/or SD-OCT suggests that vitreoretinal interface disease (eg. vitreoretinal traction or epiretinal membrane) is the primary cause of the macular edema. 11. Media clarity, pupillary dilation, and patient cooperation sufficient for adequate fundus photos. 12. No ocular condition (other than diabetes) that, in the opinion of the investigator, might affect macular edema or alter visual acuity during the first 12 months of the study (e.g., vein occlusion, uveitis or other ocular inflammatory disease, neovascular glaucoma, Irvine-Gass Syndrome). * Glaucoma per se is not an exclusion Exclusion Criteria: 1. History of renal failure requiring dialysis or renal transplant 2. Condition that in the opinion of the investigator would preclude participation in the study (e.g., unstable medical status including blood pressure and glycemic control) 3. Patients in poor glycemic control who recently (\>3 months) initiated intensive insulin treatment (a pump or multiple daily injections) or plan to do so in the next 3 months should not be enrolled. 4. A patient with only one functioning eye (i.e., letter score 0 in contra-lateral eye)