Status:

TERMINATED

Prospective,Randomized,Controlled Study to Assess Efficacy,Safety, and Tolerability of SLT vs. PLT in Patients With POAG

Lead Sponsor:

University Hospital, Geneva

Conditions:

Glaucoma and Ocular Hypertension

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

A prospective, randomized, controlled study to assess efficacy, safety, and tolerability of selective laser trabeculoplasty vs. pattern laser trabeculoplasty in patients with open-angle glaucoma.

Detailed Description

This is a prospective, randomised, controlled study. Patients will be selected for this study who require bilateral laser trabeculoplasty for IOP control. Eyes will undergo a medication wash-out 4 wee...

Eligibility Criteria

Inclusion

  • Diagnosis of open angle glaucoma (OAG) including pseudo-exfoliative and pigmentary glaucoma
  • Patients requiring bilateral laser trabeculoplasty for IOP control
  • Structural glaucomatous damage and/or documented glaucomatous VF damage (in the previous 12 months with mean defect (MD) \> 2.5 dB
  • No or stable anti-glaucomatous drug therapy since at least 3 months. Able to undergo medication washout for 4 weeks prior to baseline 24-h IOP monitoring session.
  • Aged ≥18 years, of either sex
  • Not more than 6 diopters spherical equivalent on the study eye
  • Have given written informed consent, prior to any investigational procedures

Exclusion

  • Refractory glaucoma
  • Patients having undergone ocular laser procedures (SLT, LPI) or intraocular surgery for the treatment of glaucoma.
  • Corneal or conjunctival abnormality precluding contact lens adaptation
  • Severe dry eye syndrome
  • Patients with allergy to corneal anesthetic
  • Patients with contraindications for silicone contact lens wear
  • Patients not able to understand the character and individual consequences of the investigation
  • Participation in other clinical research within the last 4 weeks
  • Any other contra-indication listed in the CLS (SENSIMED Triggerfish) user manual

Key Trial Info

Start Date :

April 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2016

Estimated Enrollment :

29 Patients enrolled

Trial Details

Trial ID

NCT02231515

Start Date

April 1 2014

End Date

June 1 2016

Last Update

May 18 2023

Active Locations (1)

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Hôpitaux Universitaires de Genève, Ophtalmology Department

Geneva, Switzerland