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Intraocular Pressure clinical trials

View clinical trials related to Intraocular Pressure.

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NCT ID: NCT02448043 Completed - Clinical trials for Intraocular Pressure

Cutaneous Prostaglandin Application: Nail Growth, Nail Brittleness, and Eye Pressure

Start date: June 4, 2015
Phase: N/A
Study type: Interventional

Topical prostaglandin agents are used to help reduce eye pressure in glaucoma patients. Bimatoprost (Lumigan 0.01%) is such an agent (Allergan, Inc.). Several of our patients on bimatoprost and an observational study of patients on bimatoprost in another center reported that fingernails grew longer and became less brittle using the topical eye drops to the eyes. The purpose of the double-blinded study is to determine whether the application of the eye drops directly to the proximal nail fold of one hand using the opposite hand as a control will result in longer nails, less brittle nails, and reduced eye pressures should any of the medication be absorbed into the systemic circulation.

NCT ID: NCT02321722 Completed - Clinical trials for Intraocular Pressure

The Effect of Colonoscopy on Intralocular Pressure

Start date: January 2015
Phase:
Study type: Observational

Glaucoma is an eye disease that damages the optic nerve, it cause blindness if not diagnosed and treated properly. The major risk factor for the development and progression of glaucoma is increased intraocular pressure. Colonoscopy is one of the most preformed world wide screening exam. It is used to detect colon cancer at its early stages. As part of this examination, the examiner inflates the inspected colon with air in order to increase the colon lumen for better visualization of the colon. As a consequence of the insufflation the intrabdominal pressure increases as well. the increase in intrabdominal pressure could increase intraocular pressure. The aim of this study is to evaluate the intraocular pressure increase while preforming colonoscopy.

NCT ID: NCT02138279 Completed - Clinical trials for Intraocular Pressure

Comparative Study of Non-contact Tonometers for Intraocular Pressure and Corneal Cell Thickness Measurements

Start date: April 2014
Phase:
Study type: Observational

The primary objective of this clinical study is to collect clinical data to support FDA 510(k) submissions for the Topcon CT-800, CT-1, CT-1P and TRK-2P non-contact tonometers. The secondary objective is to evaluate any adverse events found during the clinical study.

NCT ID: NCT02136589 Completed - Clinical trials for Intraocular Pressure

Effect of NSAID on Travoprost-induced Conjunctival Hyperemia and IOP Reduction in Normal Eyes

ENTICHIR
Start date: September 2008
Phase: Phase 4
Study type: Interventional

PG-analogues induce hyperemia as one of side effects in addition to IOP reduction. IOP reduction is caused by direct FP receptor stimulation, but the cause of hyperemia is not clarified. Because FP receptor stimulation induce intrinsic production of PGs, hyperemia or IOP reduction may be due to secondary induced PGs. Thus, pretreatment with NSAID may affect the PG-analogue induced hyperemia or IOP reduction.

NCT ID: NCT02105311 Completed - Clinical trials for Intraocular Pressure

Effect of Selective Laser Trabeculoplasty Versus Travoprost on Circardian Intraocular Pressure

Start date: March 2014
Phase: Phase 4
Study type: Interventional

The investigators conduct this study to access the effect of selective laser trabeculoplasty on 24-hour circadian tension curves of patients with open-angle glaucoma, normal tension glaucoma and ocular hypertension. This treatment effect is compared with that of the prostaglandin analogue, travoprost.

NCT ID: NCT02061644 Completed - Clinical trials for Intraocular Pressure

Spinal Anesthesia - Intraocular Pressure

Start date: March 2014
Phase: N/A
Study type: Interventional

We aim to investigate the effect of spinal anesthesia on intraocular pressure.

NCT ID: NCT01998568 Completed - Clinical trials for Intraocular Pressure

The Intraocular Pressure Measured by Different Tonometers in Corneal Edema

Start date: November 2013
Phase: N/A
Study type: Observational

The investigators conduct this study to access the effect of corneal edema (the investigators are particularly interested in those who have the clinical central corneal edema) on the variation of intraocular pressure values measured by 3 commercial-available tonometers compare to the current gold standard tonometer; Goldmann applanation tonometer.

NCT ID: NCT01995890 Completed - Clinical trials for Intraocular Pressure

Effect of Nepafenac Eye Drops on Intraocular Pressure in Normal Eyes

Start date: December 2012
Phase: Phase 4
Study type: Interventional

The Nevanac product information insert says that it can cause increase in eye pressure in 5-10% of patients. There is very little published literature on the effect of topical Nepafenac eye drops on eye pressure in normal people. The purpose of our study is to report this effect with a working hypothesis that there is no increase in eye pressure following use of Nepafenac eye drops.

NCT ID: NCT01925391 Completed - Anesthesia Clinical Trials

The Measurement of Intraocular Pressure in Normal Children Under General Anesthesia With and Without Nitrous Oxide and Anesthetic Eye Drops

IOP
Start date: January 2013
Phase: Phase 0
Study type: Interventional

Pediatric glaucoma is a rare but potentially blinding condition where the pressure in the eye is too high. Diagnosis is based on intraocular pressure (IOP) and assessment of the optic nerve, cornea and other structures. Accurate intraocular pressure measurements in young children is often impossible to obtain in an office setting. Children need sedation or general anesthesia to determine IOP. All volatile general anesthetics affect the IOP. Nitrous Oxide, a weak volatile anesthetic, does not affect IOP in healthy adults. Since Nitrous Oxide has shown to be safe and effective in a variety of practice environments, we want to evaluate the use of nitrous oxide in oxygen to obtain IOP measurements in children.

NCT ID: NCT01915680 Completed - Glaucoma Clinical Trials

Intraocular Pressure Fluctuation in Patients With Glaucoma and in Healthy Patients During Standard Yoga Positions

Start date: June 2013
Phase:
Study type: Observational

The purpose of the study is to investigate the IOP difference between normal and glaucomatous eyes using standard ophthalmic tonometry devices while subjects are performing different standard yoga asanas. The IOP of participants will be measured prior, immediately at start of the asana, 2 minutes into the asana, and immediately after assuming a sitting position. The patient will wait 10 minutes and a final IOP will be taken. Four standard yoga asanas will be tested.