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NCT05801471Recruiting

Clinical Evaluation of Visual Field Change in Glaucoma: an Assessment of Different Models of Progression

An Observational Prospective Longitudinal Study for the Clinical Evaluation of Visual Field Change in Glaucoma. An Assessment of Different Models of Progression

Source: ClinicalTrials.gov · Last updated 2 Jan 2026

Brief summary (registry, in English)

The purpose of this observational study is to collect over time a series of data in patients with glaucoma in order to evaluate different approaches in defining the progression of this pathology. These data will be collected in repeated visits over a 36-months follow-up period. At each visit, the COMPASS fundus perimeter and the Humphrey Field Analyzer (HFA) perimeter will be used to assess retinal functionality; an Optical Coherence Tomography (OCT) examination will also be performed to evaluate and obtain clinical information about the structure of the retina.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
7 Mar 2023
Start date
6 May 2022
Primary completion date
6 Nov 2028
Lead sponsor
Centervue SpA
Diseases
Glaucoma
NCT number
NCT05801471

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 6 May 2022 to the primary completion date, 6 Nov 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any ocular surgery, except for: uncomplicated cataract surgery and/or glaucoma surgery in both eyes performed within 6 months before enrollment;
  • Use of any drug that can interfere with the correct execution of perimetry or that would produce visual field loss;

Other

  • Any ocular pathology that can affect visual field other than glaucoma;
  • Inability to obtain reliable perimetric examinations;
  • Patients with advanced glaucoma for whom, according to the clinician, a 24-2 grid is not advisable to correctly monitor the patient.

Who the study is looking for

  • Glaucomatous optic nerve head in both eyes;
  • Age between 40 and 90 years;
  • Best Corrected Visual Acuity ≤ 0.3 \[logMar\];
  • Spherical refraction between -6D and +6D;
  • Astigmatism between -2D and +2D.

Age in the registry: 40 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clinica oculistica Ospedale San Paolo
Coordinator of this site? Confirm its status
MilanItalyRecruiting
Glaucoma Research Center, IRCCS Fondazione "G.B. Bietti"
Coordinator of this site? Confirm its status
RomaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.