The Sam Rothberg Glaucoma Center Goldschleger Eye Institute Sheba meical Center
Ramat Gan, 52621, Israel
NCT Number: NCT01383525
The trial objectives are to establish the safety & efficacy of using a DLTP laser to perform laser trabeculoplasty to reduce Intraocular Pressure (IOP) in patients with open angle glaucoma (Including Pigmentary & Exfoliative Glaucoma), that did not achieve adequate IOP control by conventional therapy.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Ramat Gan, 52621, Israel
This is a single site outpatient feasibility study assessing the safety & efficacy of the DLTP laser in the ability to reduce IOP in patients with open angle glaucoma (OAG). The investigational site will accrue patients with uncontrolled OAG. These eyes will be treated with the direct application of Direct Laser Trabeculoplasty (DLTP)/ Direct Selective Laser Trabeculoplasty automated device (DSLT).
Only one eye per patient is to be treated with the investigational device during the study.
The laser parameters used will be like these used in the Selective trabeculoplasty (SLT) device (CE/FDA approved), but all laser beams will be applied in about one-second, through the peri-limbal.
Subjects will be evaluated preoperatively and postoperatively at 1 hour, 2 hours (and hourly to 4 hours in the event of an IOP elevation in the immediate postop course), 1 day, 1 week, and 1, 3, 6 months.
Patients will be followed out to 6 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will be treated with a Direct Selective Trabeculoplasty (DLTP) laser. Placement of the spots is on the sclera around the limbus.
Time frame: 1,3 month
Percentage reduction of intra-ocular pressure following the non contact selective laser trabeculoplasty treatment
Time frame: 6 months
Percentage reduction of intra-ocular pressure following the non contact selective laser trabeculoplasty treatment
Time frame: 6 months
Number of medications after treatment, as compared to before treatment.
Time frame: 1 month
Physician perception of the usability of the system.
BelkinVision
Industry
Direct Application of Selective Laser Trabeculoplasty in Open Angle Glaucoma . Single Site Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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