Diabetic Retinopathy Clinical Trial
Official title:
Evaluation of the Effect of a Therapy With INTRAVIT® Tablets on Retinal Edema, Retinal Sensitivity and Visual Acuity in the Course of Diabetic Retinopathy
Verified date | February 2021 |
Source | University of Molise |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Evaluation of the effect of a therapy with INTRAVIT® tablets, on retinal edema considering also the central retinal sensitivity (Microperimetry) and the visual acuity in course of diabetic retinopathy.
Status | Active, not recruiting |
Enrollment | 40 |
Est. completion date | March 8, 2021 |
Est. primary completion date | March 8, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 70 Years |
Eligibility | Inclusion Criteria: - Diabetes type I and type II patients; - Between 20 and 70 years of age; - Age of diabetes not less than 5 years and not more than 15; - Mild non-proliferating diabetic retinopathy, limited to the presence of some microaneurysms; - Patients in diabetic compensation; - Visual acuity 5/10 natural or correct; - Patients even if hypertensive, with or without anti-hypertensive therapy in place, provided they are compensated; - Patients with good visualization of the ocular fundus. Exclusion Criteria: - Patients with concurrent eye diseases outside diabetic retinopathy; - Patients with less than natural or correct 5/10 visual acuity; - Patients treated with other vasoprotective and antioxidant preparations or having taken them in the last month; - Patients with significant systemic or metabolic diseases, except diabetes; - Patients with unbalanced Diabetes disorder; - Patients undergoing laser treatment or eye surgery (e.g. cataract); - Patients who take or should take, during the observation period, preparations for direct or indirect activity on the retina of the type that can be superimposed on INTRAVIT ®. |
Country | Name | City | State |
---|---|---|---|
Italy | University of Molise | Campobasso |
Lead Sponsor | Collaborator |
---|---|
University of Molise |
Italy,
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Wilkinson CP, Ferris FL 3rd, Klein RE, Lee PP, Agardh CD, Davis M, Dills D, Kampik A, Pararajasegaram R, Verdaguer JT; Global Diabetic Retinopathy Project Group. Proposed international clinical diabetic retinopathy and diabetic macular edema disease sever — View Citation
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | number of participants with signs of improvement/worsening of diabetic retinopathy | report presence/absence of signs with Yes/NO relative to: microaneurysms, haemorrhages, soft exudates, hard exudates, venous beading, IRMA, new vessels on optical discs, new vessels outside the optical discs, cystoid edema, capillary occlusions, degenerative alterations and vein size. | 6 months | |
Primary | number of participants in a certain stage of diabetic retinopathy according to the ETDRS modified AAO 2003 | careful evaluation of funduscopic signs (e.g exudates, neovases, micronaneurysms) to be able to stadiate patients | 6 months | |
Primary | number of patients with improved/worsened visual acuity | visual acuity measurement with ETDRS boards. The number of letters seen by the patient at each check-up visit will be noted. | 6 months | |
Primary | number of patients with improved/worsened macular edema | Foveal thickness (measured with Optical Coherence Tomography) at each check-up visit will be noted. | 6 months | |
Secondary | number of patients with improved/worsened blood parameters related to diabetes | blood sugar (mg/dl) using a rapid glucose test at each check-up visit will be noted and glycated hemoglobin (%) will be assesed with venous blood sampling at the beginning of the study and at 3 and 6 months. | 6 months |
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