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Effect of Peripheral Laser Iridotomy Placement on Post-operative Visual Function

Effect of Peripheral Laser Iridotomy Placement on Post-operative Visual Function

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03352492
Enrollment
200
Registered
2017-11-24
Start date
2018-01-01
Completion date
2021-02-28
Last updated
2020-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma, Angle-Closure

Brief summary

To evaluate the influence of superior versus temporal laser peripheral iridotomy location on post-operative visual acuity and contrast sensitivity.

Interventions

PROCEDURESuperior laser peripheral iridotomy

Iridotomy placement between 11:00 and 1:00 o'clock

PROCEDURETemporal laser peripheral iridotomy

Iridotomy placement at 3:00 or 9:00 o'clock

Sponsors

University of the Incarnate Word
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Masking description

Subject is masked to which eye has the iridotomy at which location

Intervention model description

Paired eye

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Angle-closure glaucoma * Angle-closure glaucoma suspect

Exclusion criteria

* Monocular status * Previous intraocular surgery * Visual acuity worse than 20/40 * Prior episode of acute angle-closure glaucoma * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Change in visual acuity30 days post-operativeChange from baseline best corrected visual acuity evaluated in number of letters correctly read on the ETDRS chart

Secondary

MeasureTime frameDescription
Change in Peli-Robson contrast sensitivity30 days post-operativeChange from baseline in contrast sensitivity evaluated in number of letters correctly read on the Peli-Robson chart
Change in CSV-1000 contrast sensitivity30 days post-operativeChange from baseline in contrast sensitivity evaluated using the number of correct responses on the CSV-1000 test

Countries

United States

Contacts

Primary ContactAna Hagendorf, PhD
wandless@uiwtx.edu210-805-3036

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026