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Completed

NCT Number: NCT06829810

Long-term Outcomes of Glaucoma Surgery in a Real-life Setting: the Agora Registry Study

Retrospective cohort study performed at Bordeaux University Hospital, which aims to analyze long-term safety and efficacy of different techniques of glaucoma surgery including filtering glaucoma surgeries, glaucoma drainage devices or minimally invasive glaucoma surgeries. All patients operated on in the department in the standard of care were proposed to be included in the AGORA registry study. The main outcome will be to define a modelisation of IOP profile based on the surgical technique. Secondary outcomes will be to analyze factors influencing IOP evolution as well as long-term safety and efficacy outcomes of the included surgical techniques.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU Bordeaux

Bordeaux, France

About this study

Glaucoma is a progressive degenerative optic neuropathy characterized by excavation of the optic nerve and the appearance, deepening and widening of visual field deficits (scotomas). It is the leading cause of irreversible blindness in France and worldwide. Although glaucoma is a progressive degenerative optic neuropathy with a multifactorial mechanism, all therapeutic studies have shown that lowering intraocular pressure (IOP) remains the only modulable causal factor that can stabilize or slow disease progression. It is also estimated that the glaucoma population requiring a surgery is approximately 5-10%. There is a wide range of surgical techniques for lowering IOP including filtering surgeries (trabeculectomy, non penetrating deep sclerectomy), glaucoma drainage devices and minimally invasive glaucoma surgeries. All these surgeries are acknowledged to reduce intraocular pressure but are also associated with risk of severe perioperative complications depending on glaucoma severity or ophthalmological characteristics. In addition some of them require additional procedures to maintain treatment success. These additional procedures are the consequence of IOP fluctuations over time following glaucoma surgeries. Although IOP is the main factors to control glaucoma over time, these real-life IOP fluctuations limit the use and the interpretability of survival analysis for long-term outcomes of each surgical procedure.

The aim of this study is to define a modelisation of IOP profile based on the surgical techniques and to analyze factors influencing IOP evolution as well as long-term safety and efficacy outcomes of the included surgical techniques. Demographical, ophthalmological, surgical parameters and all follow-up visits data will be collected in the standard of care of all patients who accepted to be included in the AGORA registry study. From November 2010 to April 2023, 2420 surgical procedures were recorded in the registry including 1584 Non penetrating deep sclerectomy, 212 trabeculectomy, 354 Istent or 95 high Intensity Focused Ultrasound. IOP evolution over time will be described for each surgical technique and a statistical model will be defined.

The modelisation of IOP with time and the description of risk factors of success or failure over the long-term of each surgical technique should help clinicians to make a more personalized surgical decision in order to maintain visual performances of glaucoma patients with time.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients over the age of 18 with glaucoma or ocular hypertonia treated in the ophthalmology department of Bordeaux University Hospital between 2011 and 2022.

Exclusion criteria

  • Refusal to participate
  • Patients physically or psychologically unable to understand the study and the research protocol
  • Patients under legal protection

Treatment and study plan

Modelisation of intraocular pressure profile

Other

Modelisation of IOP profile of all surgical techniques and additional procedures during the follow-up

Primary outcomes

  1. Modelisation of IOP profile

    Time frame: Baseline

    Modelisation of IOP profile of all surgical techniques and additional procedures during the follow-up

Secondary outcomes

  1. Modelisation of IOP profile of Non-perforating deep sclerectomy

    Time frame: Baseline

    Modelisation of IOP profile of Non-perforating deep sclerectomy

  2. Modelisation of IOP profile of Trabeculectomy

    Time frame: Baseline

    Modelisation of IOP profile of Trabeculectomy

  3. Modelisation of IOP profile of Glaucoma drainage device

    Time frame: Baseline

    Modelisation of IOP profile of Glaucoma drainage device

  4. Modelisation of IOP profile of MIGS Istent

    Time frame: Baseline

    Modelisation of IOP profile of MIGS Istent

  5. Modelisation of IOP profile of MIGS XEN

    Time frame: Baseline

    Modelisation of IOP profile of MIGS XEN

  6. Modelisation of IOP profile of High Intensity Focused ultrasound

    Time frame: Baseline

    Modelisation of IOP profile of High Intensity Focused ultrasound

  7. Modelisation of IOP profile of CycloDiode

    Time frame: Baseline

    Modelisation of IOP profile of CycloDiode

Sponsors and collaborators

Lead sponsor

University Hospital, Bordeaux

Other

Registry information

Acronym: GLAUCOSURG

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 17, 2025
Registry last updated
Mar 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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