View clinical trials related to Ocular Hypertension.
Filter by:Study the change of retrofoveolar choroidal thickness measured by optical coherence tomography during aerobic exercise inducing an increase in systolic blood pressure in healthy subjects.Ten healthy participants will perform an exercise (riding a bicycle ergometer) and will be examined with EDI-OCT. Each participant will be scanned before exercise, during the exercise and afterwards at 0 and 5 min. Each OCT measurement will be coupled to the arterial blood pressure evaluation.
Glaucoma is the most frequent cause of irreversible & preventable blindness worldwide, affecting about 2% of the world's population in people over 40. The major risk factor, and only treatable factor in glaucoma, is increased intraocular pressure (IOP). IOP reduction can slow or arrest the progression of vision loss. Current treatment consists of drops administered on a daily basis with unfortunately low patient compliance, increasing the chance of blindness. Eximore's product aims to eliminate the need to apply eye drops on a daily basis and thus solves the significant problem of patient compliance.
The purpose of this study is to examine whether the intraocular pressure of operated people under general anesthesia is affected by the artificial respiration method. If it is proven that there is such influence, the findings may lead to select the best method for patients with increased intraocular pressure. In this study, the investigators will monitor the changes observed in intraocular pressure caused during an operation in two different artificial respiration methods: 1. Intermittent positive pressure ventilation (IPPV) 2. High frequency jet ventilation (HFJV) Study recruited 50 patients aged 18 - 40, candidates to elective orthopedic surgery in the limbs. These patients do not suffer from general diseases that restrict their daily functioning. The selection of the type of surgery was done to prevent the involvement of any other factor, except the respiration method, determination of intraocular pressure. Exclusion Criteria: - Patients who are unable to provide an Informed Consent - Patients suffering from any eye disease - Patients with corneal thickness less than 450 microns or more than 600 microns - Smokers - Patients with pulmonary disease restrictive or obstructive - Patients using bronchodilator All patients operated under general anesthesia using total intravenous anesthesia )TIVA) method. All patients will be resuscitating half of the time of surgery using IPPV, and in the second half of surgery using HFJV. During the surgery the IOP will be measured by an ophthalmologist who is unaware of the respiration method. Correction will be made to the intraocular pressure values, depending on the thickness of the cornea. The results of the measurements will be collected and the clinical significance will be reviewed by acceptable statistical methods.