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

U

University of the Incarnate Word

Status

Unknown

Conditions

Glaucoma, Angle-Closure

Treatments

Procedure: Superior laser peripheral iridotomy
Procedure: Temporal laser peripheral iridotomy

Study type

Interventional

Funder types

Other

Identifiers

NCT03352492
16-02-003

Details and patient eligibility

About

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

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

200 participants in 2 patient groups

Bilateral iridotomy: Superior
Experimental group
Description:
Each subject in this single-arm study undergoes bilateral laser peripheral iridotomy surgery. Each participant will undergo superior laser peripheral iridotomy in one eye and temporal laser peripheral iridotomy in the fellow eye.
Treatment:
Procedure: Superior laser peripheral iridotomy
Bilateral iridotomy: Temporal
Experimental group
Description:
Each subject in this single-arm study undergoes bilateral laser peripheral iridotomy surgery. Each participant will undergo superior laser peripheral iridotomy in one eye and temporal laser peripheral iridotomy in the fellow eye.
Treatment:
Procedure: Temporal laser peripheral iridotomy

Trial contacts and locations

1

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Central trial contact

Ana Hagendorf, PhD

Data sourced from clinicaltrials.gov

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