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CompletedNCT07830017Updated Sep 21, 2026

Combined Nasal Goniotomy-Temporal Trabeculotomy Versus Temporal Trabeculotomy for Management of Primary Congenital Glaucoma

An interventional study of combined Nasal goniotomy-Temporal trabeculotomy and Temporal trabeculotomy in Primary Congenital Glaucoma, sponsored by Zagazig University. Completed at 1 site in Egypt. Open to participants aged 1 Day to 2 Years. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by Zagazig University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 3 months after the study started (first participant enrolled Feb 2024, registered May 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
21
Allocation
Randomized
Ages
1 Day to 2 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 11 studies in Hydrophthalmos with a site in Egypt — none open to participants now, 1 under way, none of them phase 3. Hydrophthalmos · Egypt.

Enrollment
9th of 10
21 · median 33
Started
2024
with 2 others
No phase
9 of 11
none open now
Registered
10th of 11
by date
Lead sponsor
1 of 11
Zagazig University

Among the 11 studies in Hydrophthalmos with a site in Egypt, this one is the 9th largest by enrollment of the 10 interventional ones that give a count, is one of 3 that started in 2024, is one of 9 with no phase, and was the 10th registered.

Hydrophthalmos

37 studies on the registry are indexed under Hydrophthalmos; 3 are open to participants now.

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Open to participants now

None of the 11 studies in Hydrophthalmos with a site in Egypt is open now. The open studies under Hydrophthalmos, anywhere →

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Download CSVNarrow it in search →With an account: the 11 studies in Hydrophthalmos with a site in Egypt as a file.
02

Study summary

Combined nasal goniotomy and temporal trabeculotomy provides effective IOP control in PCG while preserving the superior conjunctiva for future filtering procedures. By expanding the treated angle area and sparing the superior conjunctiva, this operation provides a synergistic approach that may improve long-term management strategies for pediatric glaucoma

Read the detailed description

Primary congenital glaucoma (PCG) is the main category of primary childhood glaucoma. Classically, PCG presents with one or more of the following clinical manifestations: increased corneal diameters, corneal opacification, photophobia, and excessive tearing. The increased intraocular pressure (IOP) in PCG is mainly due to an immature anterior chamber (AC) angle with inadequate aqueous filtration through the trabecular meshwork (TM). 1 Reduction of IOP in PCG relies mainly on surgical treatment. Wide variations in surgical procedures exist for the treatment of PCG, with different principles and steps. The idea behind angle-based surgeries is to remove the main barrier to aqueous filtration and create a direct pathway for aqueous to reach the Schlemm's Canal (SC). Other surgeries, such as trabeculectomy or implantation of Glaucoma drainage devices (GDD), divert the aqueous drainage toward the sub-tenon space away from the occluded TM.2,3 and 4 PCG treatment may entail the need for more than one surgery to correct the IOP. Combining two or more surgical procedures in the same setting may produce a synergistic effect in reducing the IOP while reducing the psychological and surgical burden on PCG patients. In the combined Nasal Goniotomy-Temporal Trabeculotomy (NGTT) procedure, preservation of the superior conjunctiva is an advantage that increases the success rates of further surgeries if needed. 5 In this study, the authors studied a real-world comparison between NGTT and single-site trabeculotomy for the management of PCG patients.

03

Conditions studied

  • Primary Congenital Glaucoma

Keywords

  • Glaucoma, Congenital, Trabeculotomy, Goniotomy
04

Who can participate

Ages eligible
1 Day to 2 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Child with primary congenital glaucoma

Exclusion criteria

Exclusion Criteria:

  • associated ocular diseases other than glaucom
  • posterior segment congenital anomalies
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
21 participants (actual)

Study arms

  • Active comparator
    combined Nasal goniotomy-Temporal trabeculotomy

    combined nasal goniotomy-Temporal trabeculotomy

    Procedure: combined Nasal goniotomy-Temporal trabeculotomy

  • Active comparator
    Temporal trabeculotomy

    Temporal trabeculotomy

    Procedure: Temporal trabeculotomy

Interventions

  • Procedurecombined Nasal goniotomy-Temporal trabeculotomy

    Temporal trabeculotomy

  • ProcedureTemporal trabeculotomy

    Temporal trabeculotomy

06

What researchers measure

Primary outcomes

  1. intra ocular pressure

    post operative IOP compared to preoperative IOP

    Time frame: 1 YEAR

07

Study locations

1 site
  • Zagazig University
    Zagazig, Sharqia Province 44511, Egypt
08

References and documents

Publications

  • Anderson DR. Trabeculotomy compared to goniotomy for glaucoma in children. Ophthalmology. 1983 Jul;90(7):805-6. doi: 10.1016/s0161-6420(83)34484-5. PubMed 6622020 ↗

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Feb 2024 to primary completion in Feb 2026, 24 months.

Of 11 interventional studies with no phase under Hydrophthalmos, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 22 and three quarters within 25. This study's 24 months is close to that.

How these figures are worked out, and which studies are left out of them.

Registered
May 23, 2026
First posted
Sep 21, 2026
StartActual
Feb 1, 2024
Primary completionActual
Feb 1, 2026
CompletionActual
Feb 1, 2026
Last update
Sep 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07830017
Lead sponsor
Zagazig University
Responsible party
Mohammed Alsaeed Al Naimy Habeeb (Professor, Zagazig University) — Principal investigator
First posted
Sep 21, 2026
Start date
Feb 1, 2024
Primary completion
Feb 1, 2026
Completion
Feb 1, 2026
Last update
Sep 21, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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