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OpenTrials
Completed

NCT Number: NCT01383525

Direct Application of Selective Laser Trabeculoplasty in Open Angle Glaucoma

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Sam Rothberg Glaucoma Center Goldschleger Eye Institute Sheba meical Center

Ramat Gan, 52621, Israel

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient is aged 18 years or older, with 2 sighted eyes.
  • Eye to be treated have average IOP *22 mmHg, measured at 2 pretreatment visits.
  • Eye to be treated either exhibits:
  • poorly controlled open angle glaucoma including Pigmentary & Exfoliative Glaucoma
  • Patient would be considered eligible for conventional laser trabeculoplasty.
  • Patient is willing to participate in the 6-month study and to adhere to the follow-up schedule.
  • Patient is willing to review and sign a consent form.

Exclusion criteria

  • evidence of glaucoma other than open-angle glaucoma;
  • severe para-central or generalized field defect;
  • Any ocular condition that precluded adequate visualization and treatment of the trabecular meshwork.
  • Prior glaucoma surgery other than laser trabeculoplasty or peripheral iridotomy.
  • Patient has mental impairment such that he/she could not understand the protocol or is not in a position to provide written informed consent.
  • Patient is pregnant.
  • Patient might require other ocular surgery within the 6-month follow-up period.
  • Patient has a medical history that suggested the potential for complications from Direct Selective Trabeculoplasty (DSLT)
  • Having concurrent treatment with systemic steroids.
  • Patient is under 18 years old

Treatment and study plan

Direct Selective Trabeculoplasty device

Device

Patients will be treated with a Direct Selective Trabeculoplasty (DLTP) laser. Placement of the spots is on the sclera around the limbus.

Primary outcomes

  1. Reduction of Intra-Ocular pressure

    Time frame: 1,3 month

    Percentage reduction of intra-ocular pressure following the non contact selective laser trabeculoplasty treatment

Secondary outcomes

  1. Reduction of Intra-Ocular pressure

    Time frame: 6 months

    Percentage reduction of intra-ocular pressure following the non contact selective laser trabeculoplasty treatment

Other outcomes

  1. Number of medications

    Time frame: 6 months

    Number of medications after treatment, as compared to before treatment.

  2. Physician perception of the usability of the system.

    Time frame: 1 month

    Physician perception of the usability of the system.

Sponsors and collaborators

Lead sponsor

BelkinVision

Industry

Collaborators

  • Horizon 2020 - European Commission

Registry information

Official study title

Direct Application of Selective Laser Trabeculoplasty in Open Angle Glaucoma . Single Site Study

Important dates

Study start
2011
Primary completion
2019
Study completion
2019
First posted
Jun 28, 2011
Registry last updated
Feb 26, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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