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Retinal Vascular Reactivity in Subjects With Newly Diagnosed Glaucoma Before and After Selective Laser Trabeculoplasty

U

University of Toronto

Status

Unknown

Conditions

Glaucoma

Treatments

Procedure: Selective Laser Trabeculoplasty

Study type

Observational

Funder types

Other

Identifiers

NCT01209975
SLT-blood flow study

Details and patient eligibility

About

The purpose of this study is to assess retinal blood flow and vascular reactivity in patients with newly diagnosed primary open angle glaucoma pre- and post-primary Selective Laser Trabeculoplasty(SLT). Canon Laser Blood Flowmeter will be used for the assessment of retinal blood flow.

Full description

We previously found that vascular reactivity improved after short term treatment with dorzolamide drops. It is not clear whether this improvement was a direct effect of the medication or secondary effect of the decrease in IOP. We would like to see the change of vascular reactivity before and after SLT, which will decrease the intraocular pressure without pharmacologic effect.

Enrollment

12 estimated patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 40-75 years (Male or Female)
  2. Best corrected visual acuity of at least 20/40
  3. No previous treatment for glaucoma
  4. Ametropia less than ±6.0 DS and ±2.5 DC)
  5. Non-smoker
  6. No cardiovascular/respiratory disorders

Exclusion criteria

  1. Past history of diabetes and cerebrovascular accident
  2. Vascular occlusive disease affecting the ocular circulation such as: diabetic retinopathy, retinal vein occlusion and retinal artery occlusion
  3. Previous intraocular surgery
  4. Ocular media opacities limiting the use of the imaging tests

Trial design

12 participants in 1 patient group

untreated glaucoma patients
Description:
We will evaluate the blood flow before and after Selective Laser Trabeculoplasty in patients with primary open angel glaucoma.
Treatment:
Procedure: Selective Laser Trabeculoplasty

Trial contacts and locations

1

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Central trial contact

Tien Wong

Data sourced from clinicaltrials.gov

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