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Neuropathy, Optic clinical trials

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NCT ID: NCT05931250 Recruiting - Cerebral Injury Clinical Trials

Alternating and Direct Current Stimulation for Neuropathic Eye Pain

Start date: June 16, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical intervention is to test if two forms of transcranial current stimulation, transcranial direct current stimulation (tDCS) or transcranial alternating current stimulation (tACS) can alleviate neuropathic eye pain in a sample of 20 patients. The main aims are: - Test if tDCS/tACS can alleviate neuropathic eye pain and/or other cerebral symptoms: brain fatigue, migraine, light sensitivity, etc. - Test if one stimulation method is superior to the other Patients will be treated for a total of fifteen 30-minute stimulation sessions, three times a day over a five-day period, each stimulation separated by approximately 4 hours, with either active tACS or tDCS over the scalp corresponding to primary sensory and motor areas. The patients will have questionnaires to monitor subjective experiences and pupillometry before and after treatment to monitor experimental outcomes.

NCT ID: NCT03642899 Completed - Neuropathy, Optic Clinical Trials

OCT Angiography in Arteritic and Non Arteritic Anterior Ischemic Neuropathy

NOIA
Start date: August 29, 2018
Phase:
Study type: Observational

Anterior ischaemic optic neuropathy results from infarction of retrolaminar portion of the optic nerve head, caused by occlusion of the posterior ciliary artery. Non arteritic anterior ischaemic optic neuropathy affects more frequently people between 50 and 70 years of age, with vasculopathic risk factors. Arteritic anterior ischaemic optic neuropathy is caused by the Horton disease, affects an older population and is an ophthalmologic emergency because of the bilateralisation's risk. The aim of this study is to compare the peripapillar vascular density of anterior ischaemic optic neuropathy eyes (arteritic and non arteritic) with normal eyes after the disappearance of the papillar edema, with oCT-angiography. The investigators will include patients with anterior ischaemic optic neuropathy and normal patients. For each participant, the investigators will estimate the best visual acuity, intra-ocular pressure, make a fondus, measurement of retinal nervous layer thickness, ganglionar cells layer thickness, and a macular and papillar OCT angiography during a consultation (duration 30 min). The investigators will be able to know if - there is a modification of the peripapillary vascularisation subsequent to the occlusion of the posterior ciliary artery - there is a difference between arteritic and non arteritic anterior ischaemic optic neuropathy, - there is a repercussion of the neuropathy on the retinal layers, - there is a difference in peripapillar vascularisation by age.