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Comparing Nd:YAG Laser and Sequential Double Frequency YAG-Nd:YAG Laser Iridotomy

Randomized Clinical Trial Comparing Neodynium:Ytrium-aluminium-garnet (Nd:YAG) Laser and Sequential Double Frequency YAG-Nd:YAG Laser Iridotomy in Patients With Dark Iris

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02474238
Enrollment
82
Registered
2015-06-17
Start date
2015-05-31
Completion date
2018-08-31
Last updated
2018-08-27

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

Conditions

Angle Closure Glaucoma

Keywords

Iridotomy

Brief summary

No single type of laser or set of laser parameters is appropriate for all type of irides. Pure Nd:YAG laser iridotomy is very effective in the light color irides. It was considered as the gold standard for iridotomy. It, however, is less effective and causes some complication such as iris hemorrhage especially in patients with dark iris.

Detailed description

By using the double frequency YAG to make the initial bore and the Nd:YAG laser to complete the perforation, the technique should be able to effectively combine most of the advantages of both lasers whilst avoiding their disadvantages. It is possibly the ideal iridotomy technique to use in the Asian irides. The investigators aim to study the energy use for laser iridotomy comparing between the two techniques as well as objectively measure the variables associated with complications.

Interventions

DEVICEThe sequential technique

By using 'the double frequency YAG laser' to make the initial bore and 'the Nd:YAG laser' to complete the perforation on iris.

DEVICEThe pure Nd:YAG laser technique

By using 'the pure Nd:YAG laser' to make a complete perforation on iris.

Sponsors

Prince of Songkla University
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Patient in need to have a laser iridotomy * primary angle closure glaucoma or * primary angle closure or * primary angle closure suspect (needed repeated pupil dilation) or * fellow eyes of acute angle closure crisis, and * Age of at least 18 years, and * Dark iris patients (only black and dark brown color)

Exclusion criteria

* Eye with acute angle closure crisis * Active conjunctiva or corneal infection or inflammation * Active anterior uveitis * History of any prior laser treatment * History intraocular surgery * Eye with corneal scar * Corneal haziness obscure iridotomy site * Endothelial cell count less than 1000 cells/mm2 (pre-laser) * Iris color other than black or dark brown * Inability to sit at the slit lamp to have laser done

Design outcomes

Primary

MeasureTime frameDescription
Laser energy1-hourTotal energy used to create patency on the iris

Secondary

MeasureTime frameDescription
Bleeding1-houriris bleeding immediate after laser reported as Yes or No
Corneal endothelial cell count12-monthCorneal endothelial cell count directly over the area of laser
Central corneal thickness12-monthCentral corneal thickness
Patency of iridotomy12-monthIridotomy patency is confirmed objectively reported as yes or no
Intraocular pressure spike1-hourIntraocular pressure spike if present mean that IOP evelation of at least 8mmHg from baseline intraocular pressure

Countries

Thailand

Outcome results

None listed

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