Persistent Diabetic Macular Edema
Conditions
Keywords
diabetic macular edema
Brief summary
The investigators would like to investigate the efficacy of more frequent treatment with Lucentis for subjects with persistent diabetic macular edema despite standard dosing regimen.
Detailed description
This is an open-label, subject masked, phase II study of intravitreally administered ranibizumab in subjects with persistent diabetic macular edema. Persistent diabetic macular edema is defined as subjects who still have central subfield thickness on SD-OCT of greater than 320 microns after having received at least 3 previous doses of AntiVEGF therapy in the past 5 months. Consented, enrolled subjects will be randomized into two subgroups: (1) standard dosing of monthly 0.3mg ranibizumab or (2) 0.3mg ranibizumab given 2 weeks apart for 5 doses followed by monthly dosing.
Interventions
DRUGranibizumab
ranibizumab 0.3mg intravitreally monthly
Sponsors
Maturi, Raj K., M.D., P.C.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Subjects will be eligible if the following criteria are met: * Ability to provide written informed consent and comply with study assessments for the full duration of the study * Age \>18 years * Diagnosis of Type 1 or Type 2 diabetes * BCVA score using the ETDRS method of \>24 and \<78 in the study eye at the screening visit * 3 or more intravitreal injections of AntiVEGF over the 5 months prior to screening * Presence of diabetic macular edema defined as SD-OCT CST \>320 microns on spectral domain machine
Exclusion criteria
* Subjects who meet any of the following criteria will be excluded from this study: * Anti-VEGF treatment in the study eye within 3 weeks prior to screening * Intravitreal Ozurdex treatment in the study eye within 12 weeks prior to screening * Intravitreal steroid treatment in the study eye within 8 weeks prior to screening * PRP or focal laser in the study eye within 4 months prior to screening * Active iris neovascularization in the study eye * Any ocular condition in the study eye that, in the opinion of the investigator, is severe enough to compromise the study result. * History of cataract surgery in the study eye within 3 months prior to screening visit * Uncontrolled systemic disease * Current enrollment in an investigational drug study or participation in such a study within 30 days prior to the screening visit * Female patients who are pregnant, nursing or planning a pregnancy or who are of childbearing potential and not using a reliable means of contraception. * Any condition or reason (including inability to read ETDRS chart or language barrier) that precludes the patient's ability to comply with study requirements including completion of the study. * Known allergy, hypersensitivity or contraindication to the study medications, its components, fluorescein or povidone iodine.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| mean change in optical coherence topography central subfield thickness at 12 weeks and 24 weeks after randomization | 24 weeks | mean change in optical coherence topography central subfield thickness at 12 weeks and 24 weeks after randomization |
Countries
United States
Outcome results
None listed