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CompletedNCT01087684Updated Oct 10, 2013

Response to SLT vs. ALT in Patients Under 60 Years of Age

An interventional study of Argon laser trabeculoplasty and Selective laser trabeculoplasty in Glaucoma, sponsored by Sunnybrook Health Sciences Centre. Completed at 1 site in Canada. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2013-10-10.

Sponsored by Sunnybrook Health Sciences Centre · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

Laser trabeculoplasty is a routine treatment for glaucoma and can be performed with either argon (ALT) or selective Yag (SLT) lasers. The effectiveness of each has not been studied in patients under 60 years, which is younger than average for the procedure. The study hypothesis is that there will be no difference between the two laser types.

Read the detailed description

Forty-two young patients (age 29 to 60) had one eye randomized to ALT (n = 22) or SLT (n = 20). Intraocular pressure was measured prior to laser and 1 hour, 1 day, 6 weeks, 3 months, every 3 months until 2 years, and then yearly post-laser. χ2 analysis and student's t-test were used to determine statistical significance.

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Conditions studied

  • Glaucoma

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Keywords

  • Glaucoma
  • laser trabeculoplasty
  • intraocular pressure
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In context

Glaucoma

1,818 studies on the registry are indexed under Glaucoma; 231 are open to participants now.

This study's enrollment of 42 is below the median of 65 across 1,272 interventional studies indexed under Glaucoma.

Browse Glaucoma studies →

Lead sponsor

Sunnybrook Health Sciences Centre is the lead sponsor of 566 studies on the registry; 134 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age \< 60 years
  • Intraocular pressure not adequately controlled

Exclusion criteria

Exclusion Criteria:

  • Prior laser treatment
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Single (Investigator)
Enrollment
42 participants (actual)

Study arms

  • Active comparator
    Argon laser trabeculoplasty

    Patients received standard argon laser treatment

    Procedure: Argon laser trabeculoplasty

  • Active comparator
    Selective laser trabeculoplasty

    Patients received a standard selective laser treatment

    Procedure: Selective laser trabeculoplasty

Interventions

  • ProcedureArgon laser trabeculoplasty

    Argon laser 600-800 mW, 0.1seconds, 50 micron spot size, 45 - 55 burns over 180 degrees of trabecular meshwork

    Also known as: ALT

  • ProcedureSelective laser trabeculoplasty

    Selective laser trabeculoplasty 0.7 - 0.8 mJ, 400 micron spot size, 3 nanosecond, 45 - 55 burns over 180 degrees of trabecular meshwork.

    Also known as: SLT

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What researchers measure

Primary outcomes

  1. Intraocular pressure

    The intraocular pressure was measured at 6 weeks, 4.5 months, 9, 12, 18 and 24 months following the laser treatment.

    Time frame: Two years

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Study locations

1 site
  • Sunnybrook Health Sciences Centre
    Toronto, Ontario M4N 3M5, Canada
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References and documents

Publications

  • Liu Y, Birt CM. Argon versus selective laser trabeculoplasty in younger patients: 2-year results. J Glaucoma. 2012 Feb;21(2):112-5. doi: 10.1097/IJG.0b013e318202791c. PubMed 21572334 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 10, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01087684
Lead sponsor
Sunnybrook Health Sciences Centre
Responsible party
Dr. Catherine Birt (MD, Sunnybrook Health Sciences Centre) — Principal investigator
First posted
Mar 16, 2010
Start date
Dec 2004
Primary completion
Dec 2008
Completion
Dec 2008
Last update
Oct 10, 2013

Study contacts

Catherine M Birt, MD
principal investigator · Sunnybrook Health Sciences Centre

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2013. You cannot join it, but the record below documents what was studied.

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