Complications of Diabetes Mellitus Clinical Trial
Official title:
The Effect of Reducing the Intraocular Pressure by Using Alphagan Drops and Macular Edema in Patients With Diabetic Macular Edema
The Investigators propose to examine the effect of lowering the intraocular pressure on macular edema in Participants diagnosed with diabetic macular edema. Our theory is based on the assumption that lower intraocular pressure means higher Ocular Perfusion pressure, which may cause an improvement in retinal perfusion and thus an improvement in retinal oxygenation and reduced edema
Status | Recruiting |
Enrollment | 25 |
Est. completion date | July 2018 |
Est. primary completion date | March 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Participants with a diagnosis of diabetic macular edema over the age of 18 which are eligible to sign an agreement to participate in the study - Presence of DME (based on clinical examination of retinal specialist + OCT) in both eyes with an edema thickness ranged from 350 to 800 microns - Media lucid enough to allow sufficient quality photographs by OCT Exclusion Criteria: - Patients which do not have a valid diagnosis of DME (Diabetic Macular Edema) - Patients with problems that can cause macular edema in any other: - Age-Related Macular Degeneration - Central retinal vein occlusion (CRVO)/Branch retinal vein occlusion (BRVO) /central retinal artery occlusion (CRAO) / branch retinal artery occlusion (BRAO) - Epiretinal membrane (ERM) or Vitreo-macular traction (VMT) - Patients who are Pseudophakic in one eye or pseudophakic in both eyes for less than a year - Patients treated in order to reduce the DME by intra-vitreal injection or by laser in the past six months - Patients which are currently treat with Intra ocular Pressure lowering drops in at least one eye, or have been treated in the past with laser of any kind or with surgery - Patients who underwent Pars plana vitrectomy one or both eyes - Patients who cannot undergo an OCT examination - Patients who want prefer to be treated by the current practices based on clinical judgment - Patients with a condition that requires an intervention or laser surgery during the 3 months of study, such as active Proliferative diabetic retinopathy, vitreous hemorrhage or other similar conditions |
Country | Name | City | State |
---|---|---|---|
Israel | Meir Medical center | Kfar Saba |
Lead Sponsor | Collaborator |
---|---|
Meir Medical Center | Meir Hospital, Kfar Saba, Israel |
Israel,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of at least 50 micron in Macular edema | The participants will be examined every month from the time of recruitment as mentioned before, at each visit the Macular Edema will be assessed, but the Outcome measure will be defined as Change of at least 50 Micron in Macular Edema at the third visit, 3 months from recruitment | Baseline measurement will be conducted at the recruitment of the participant, the second measurement will be preformed after one moth from recruitment and the third and last measurement will be preformed after 3 months from recruitment |
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