Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05366647

GATT Versus Canaloplasty (GVC)

Led by Medical University of Bialystok · Updated on 2025-03-07

100

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

M

Medical University of Bialystok

Lead Sponsor

M

Medical University of Lublin

Collaborating Sponsor

AI-Summary

What this Trial Is About

Study aims to compare the effectiveness and safety profile of Gonioscopy-assisted Transluminal Trabeculotomy and canaloplasty, in order to find out if one operation is superior to the other. Both procedures are performed in patients with medically uncontrolled open-angle glaucoma. Canaloplasty is a recently newly introduced procedure, which showed encouraging results without antimetabolite usage intra- and postoperatively. Gonioscopy-assisted Transluminal Trabeculotomy is the procedure that aims the same mechanism of aqueous outflow, however is perform with ab interno approach, which comprise it to the minimally invasive glaucoma surgery techniques. Purpose of the study is to compare both surgeries concerning success rate, intraocular pressure, medication burden and complications rate. So far there is no comparison of the Gonioscopy-assisted Transluminal Trabeculotomy and canaloplasty available.

CONDITIONS

Official Title

GATT Versus Canaloplasty (GVC)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years and older
  • Confirmed uncontrolled open-angle glaucoma
  • No prior glaucoma surgery except laser trabeculoplasty or cyclophotocoagulation
Not Eligible

You will not qualify if you...

  • Angle closure glaucoma
  • Congenital glaucoma
  • Inflammatory glaucoma

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
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Trial Site Locations

Total: 1 location

1

Ophthalmology Clinic Medical University of Bialystok

Bialystok, Poland, 15-089

Actively Recruiting

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Research Team

J

Joanna Konopińska

CONTACT

E

Ewa Kosior-Jarecka

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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