Evaluation of Pascal Laser Trabeculoplaty



Status:Completed
Conditions:High Blood Pressure (Hypertension), Ocular
Therapuetic Areas:Cardiology / Vascular Diseases, Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:4/2/2016
Start Date:March 2008
End Date:March 2010
Contact:Christopher J Engelman, MD
Email:engelman@stanford.edu
Phone:408-885-6877

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Prospective Evaluation of the Efficacy of Pascal Trabeculoplasty: A Pilot Study

Laser Trabeculoplasty has been shown to be effective in lowering intraocular pressure (IOP)
in patients with primary open-angle glaucoma (POAG). Although initially demonstrated with
the Argon laser (ALT), several other laser systems have also been employed with comparable
efficacy. Recently, Selective Laser Trabeculoplasty (SLT) has been shown to lower
intraocular pressure comparable to ALT. The advantage of SLT is that the target eye
structure, the trabecular meshwork, remains intact with minimal damage at the cellular
level. In contrast, ALT lowers IOP at the expense of scarring of the trabecular meshwork.
The purpose of this study is to evaluate the efficacy of lowering IOP with Pascal Laser
Trabeculoplasty (PLT) employing reduced energy levels compared to ALT and a computer guided
pattern of laser treatment applications.


Inclusion Criteria:

1. Otherwise healthy males and females, older than 18 years of age with two (2) sighted
eyes

2. Have OAG, PXG, or combined mechanism glaucoma - as long as their angles are open

3. Have uncontrolled IOP (>24mmHg); or controlled with Medicine(s)

4. If on medical treatment, have undergone a washout period of at least one month prior
to Pascal treatment

5. Able and willing to comply with the treatment/follow-up schedule and requirements;

6. Able to provide written informed consent

Exclusion Criteria:

1. Pregnant, intending to become pregnant during course of study, less than 3 months
postpartum or less than 6 weeks after completion of breastfeeding

2. Have an advanced visual field defect within 10° of fixation

3. Have had previous glaucoma surgery, except for peripheral iridotomy

4. Have corneal disease obviating the use of corneal applanation for a reliable IOP
measurement, or would cause difficulty in viewing the TM by means of gonioscopic lens

5. Using systemic steroids

6. Participation in a study of another device or drug within 3 month prior to study
enrollment or during this study, and as per the Investigator's careful discretion, as
long as not contradictory to any of the above criteria

7. Any condition which, in the Investigator's opinion, would make it unsafe (for the
subject or for the study personnel) to treat the subject as part of this research
study

8. No concomitant use of IOP lowering medicine (Group 1)

9. No co-existing ocular pathology with the exception of Cataract.
We found this trial at
1
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San Jose, California 95128
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San Jose, CA
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