Actively Recruiting

All Genders
NCT07454447

UBM Evaluation After Combined Deep Sclerectomy With Trabeculotomy in Primary Open Angle Glaucoma

Led by Minia University Hospital · Updated on 2026-03-06

30

Participants Needed

1

Research Sites

55 weeks

Total Duration

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AI-Summary

What this Trial Is About

Primary open-angle glaucoma is a chronic optic neuropathy that often requires surgical intervention when medical treatment fails. Deep sclerectomy is a non-penetrating glaucoma surgery that aims to reduce intraocular pressure while minimizing complications. When combined with trabeculotomy, additional aqueous outflow may be achieved. Ultrasound biomicroscopy (UBM) allows detailed imaging of the anterior segment and provides valuable information about postoperative anatomical changes that cannot be assessed clinically. This observational study aims to evaluate UBM findings after combined deep sclerectomy with trabeculotomy in patients with primary open-angle glaucoma and to correlate these findings with clinical outcomes.

CONDITIONS

Official Title

UBM Evaluation After Combined Deep Sclerectomy With Trabeculotomy in Primary Open Angle Glaucoma

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of primary open-angle glaucoma or juvenile open-angle glaucoma
  • Patients who have had combined deep sclerectomy with trabeculotomy surgery
  • Clear eye media suitable for ultrasound biomicroscopy imaging
  • Provided written informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Presence of secondary glaucoma types such as neovascular, uveitic, traumatic, or angle-closure glaucoma
  • Previous glaucoma filtering surgery in the eye being studied
  • Other eye conditions that interfere with ultrasound biomicroscopy imaging, including severe corneal opacity or scleral pathology

AI-Screening

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Trial Site Locations

Total: 1 location

1

Minia University Hospital

Minya, Minya Governorate, Egypt

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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