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Subthreshold Diode Laser Versus Trabeculotomy in Treatment of Advanced Primary Open Angle Glaucoma

Subthreshold Diode Laser Versus Trabeculotomy in Treatment of Advanced Primary Open Angle Glaucoma

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07591662
Enrollment
80
Registered
2026-05-18
Start date
2024-06-01
Completion date
2024-12-01
Last updated
2026-05-18

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

Conditions

Advanced Primary Open Angle Glaucoma, Intraocular Pressure, Subthreshold Diode Laser, Trabeculotomy

Brief summary

This study aimed to compare between subthreshold diode laser and trabeculotomy in treatment of advanced primary open angle glaucoma throughout 12 months follow-up.

Detailed description

Glaucoma is a common eye disease that can cause irreversible blindness if left undiagnosed and untreated. Glaucoma is caused by elevated intraocular pressure (IOP) that leads to optic nerve damage and visual field loss. Trabeculectomy operation was first described more than 50 years ago and is considered the most commonly performed surgery worldwide for glaucoma patients. Subthreshold transscleral cyclophotocoagulation is a micropulse delivery mode of diode laser that has been used recently to treat glaucoma by ablating the ciliary processes and reducing the aqueous humour production.

Interventions

PROCEDURESubthreshold diode laser

Patients scheduled for subthreshold diode laser.

PROCEDURETrabeculotomy

Patients scheduled for trabeculotomy.

Sponsors

Kafrelsheikh University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients older than 18 years. * Open angle glaucoma. * Advanced glaucoma (visual field deterioration MD\>-12.00 dB with evidence of optic neuropathy despite maximal therapy).

Exclusion criteria

* Previous intraocular surgery for glaucoma. * Patients who had undergone previous laser therapy for glaucoma. * Cases of secondary glaucoma. * Media opacity interferes with capturing fundus image.

Design outcomes

Primary

MeasureTime frameDescription
Visual acuity12 months postoperativelyVisual acuity was evaluated using finger counting, hand motion, or light perception

Secondary

MeasureTime frameDescription
Intraocular pressure12 months postoperativelyIntraocular pressure was measured and success criteria included an IOP ranging from 6 to 21 mmHg or a minimum 20% decline from baseline, with or without antiglaucoma drugs.
Degree of pain12 months postoperativelyPostoperative pain was assessed using a visual analogue scale from 0 to 10 cm: 0-4 cm for mild, 5-7 cm for moderate, and 8-10 cm for intense pain.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 19, 2026