Diabetes Clinical Trial
— RGCCOfficial title:
Retinal Ganglion Cell Complex Changes Using Spectral Domain Optical Coherence Tomography in Diabetic Patients Without Retinopathy
| Verified date | December 2015 |
| Source | Cairo University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Egypt: Institutional Review Board |
| Study type | Interventional |
Neuroretinal damage in diabetes produces functional abnormalities such as the loss of
chromatic discrimination,contrast sensitivity and dark adaptation. These alterations can be
detected by means of electrophysiological studies in diabetic patients with diabetes
duration of less than two years, i.e. before microvascular lesions can be detected in
ophthalmologic examination. Neurodegeneration seems to be a generalized process that occurs
throughout the macula and is not confined to local abnormalities, in the cases with visible
signs of retinopathy.
The debate is still open as to whether diabetic retinal neuropathy is the effect of vascular
diabetic retinopathy or is primarily caused by direct neurologic damage from chronic
hyperglycemia. The hypothesis that diabetes causes retinal neuro-pathy independent of
retinopathy is intriguing and potentially links retinal neuropathy to other diabetic
neuropathies.
Neuroretinal degeneration initiates and/or activates several metabolic and signalling
pathways which participates in the microangiopathic process as well as in the disruption of
the blood-retinal barrier which is a crucial element in the pathogenesis of diabetic
retinopathy.
Retinal ganglion cells are the earliest cells affected and have the highest rate of
apoptosis. However, an elevated rate of apoptosis has been also observed in the outer
nuclear layer (photoreceptors) and in the retinal pigment epithelium (RPE). The use of
spectral domain OCT (SD-OCT) makes it possible to measure the thickness of individual layers
at higher resolution and indicates that the thinning of the inner retina in the macula is
primarily due to loss of ganglion cells.
| Status | Completed |
| Enrollment | 35 |
| Est. completion date | December 2014 |
| Est. primary completion date | December 2014 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | N/A and older |
| Eligibility |
Inclusion Criteria: 1. Diabetic patients free from diabetic retinopathy will be group 1 2. Non-diabetic subjects will be group 2. Exclusion criteria included; 1. Diabetic patients with diabetic retinopathy 2. Patients having other ocular diseases as glaucoma or uveitis. 3. Eye with history of previous ocular surgeries, trauma or intraocular injections or photocoagulation. |
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic
| Country | Name | City | State |
|---|---|---|---|
| Egypt | Department Of Ophthalmology | Cairo |
| Lead Sponsor | Collaborator |
|---|---|
| Cairo University |
Egypt,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Retinal Ganglion Cell Complex in microns by Optical Coherence Tomography measurements | Baseline | No |
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