Skip to content

Optical Coherence Tomography of the Irido-Corneal Angle Before and After Goniotomy and Trabeculotomy in Primary Congenital Glaucoma

Optical Coherence Tomography of the Irido-Corneal Angle Before and After Goniotomy and Trabeculotomy in Primary Congenital Glaucoma

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07012252
Enrollment
32
Registered
2025-06-10
Start date
2018-10-01
Completion date
2020-11-01
Last updated
2025-06-10

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

Conditions

Anterior Chamber Angle, Goniotomy, Optical Coherence Tomography, Primary Congenital Glaucoma, Trabeculotomy

Brief summary

The research aimed to improve surgical techniques and long-term outcomes by utilizing this advanced imaging technology to illuminate the structural abnormalities of the anterior segment in eyes with primary congenital glaucoma.

Detailed description

Primary congenital glaucoma (PCG) is a rare disease, but it is responsible for 2.5%-15% of all documented cases of pediatric blindness. The main target of the treatment of pediatric glaucoma is to control the IOP surgically. However, medical treatment could be instituted as a temporary and/or adjunctive option to maximize Intraocular pressure (IOP) control. Initial goniotomy or trabeculotomy have been detected to have high success rates. Trabeculotomy has a comparable long-term success rate in most patients of PCG. The success rate of trabeculotomy is lower in advanced or late-presenting patients.

Interventions

PROCEDUREOptical coherence tomography

Infants underwent optical coherence tomography.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Weeks to 72 Weeks
Healthy volunteers
No

Inclusion criteria

* Age from 1 to 72 weeks. * Both sexes. * Infants with primary congenital glaucoma.

Exclusion criteria

* Eyes in which the angle could not be visualized by the handheld anterior segment optical coherence tomography (HH AS-OCT). * Eyes with previous intraocular surgery.

Design outcomes

Primary

MeasureTime frameDescription
Central corneal thickness6 months post-procedureCentral corneal thickness was measured using handheld anterior segment optical coherence tomography (HH AS-OCT).

Secondary

MeasureTime frameDescription
Trabecular-iris angle6 months post-procedureTrabecular-iris angle was measured using handheld anterior segment optical coherence tomography (HH AS-OCT).
Iris thickness6 months post-procedureIris thickness was measured using handheld anterior segment optical coherence tomography (HH AS-OCT).

Countries

Egypt

Outcome results

None listed

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