The purpose of this study is to evaluate the effectiveness and the safety of the
cyclocoagulation using High Intensity Focused Ulatrsound with the EYEOP1 device in glaucoma
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01592955
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
IOP > 21 mm Hg
No previous intraocular surgery or laser treatment during the 90 days before HIFU day
Age > 18 years
Informed consent sgned by the subject
Normal Tension Glaucoma
Glaucoma drainage device implanted and still present in the eye to be treated
History of ocular or retrobulbar tumor
Ocular infection within 14 days prior to the HIFU procedure
Ocular disease other than glaucoma that may affect assessment of visual and/or IOP
(choroidal hemorrhage or detachment, lens subluxation, thyroid ophthalmopathy, proliferative diabetic retinopathy, clinical significant macular edema)
Pregnant or breast-feeding women, or lack of contraception use among women likely to have a child
All locations for NCT01592955
The Sam Rothberg Glaucoma Center, Goldschleger EyeInstitute, Sheba Medical Center
Tel Hashomer, Israel, 52621
Ospedale San Paolo
Milano, Italy, 20142
Institute Ophthalmology - Universita di Parma
Parma, Italy, 43121
Clinica Oculistica Universitaria - P-O Oftalmico
Torino, Italy, 10149
Madrid, Spain, 28040
Hôpitaux Universitaires de Genève
Genève, Switzerland, CH-1211
Clinique de Montchoisi - Glaucoma center
Lausanne, Switzerland, CH-1006
View full eligibility
Tris trial is registered with FDA with number: NCT01592955. The sponsor of the trial is EyeTechCare and it is looking for 84 volunteers for the current phase.
Official trial title: Glaucoma Treatment by Cyclo-coagulation Using High Intensity Focused Ultrasound With the EyeOP1 Medical Device.
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