Follow up of High Myopic Eyes

In this non-interventional retrospective and prospective observational study, the long-term evolution of clinical and iconographic characteristics of patients with pathological myopia will be considered Changes of some specific clinical, tomographic and angiographic variables evaluated on the baseline and after a minimum of 5 years follow-up will be studied.

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Key information

Conditions

Pathologic Myopia

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Istituto Auxologico Italiano IRCCS

Milan, 20145, Italy

Location status: Recruiting

Location contact

Paolo Milani, MD

CONTACT

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

high myopia

Exclusion criteria

acute ischemic optic neuropathy
macular and peripapillary atrophy
other forms of maculopathy

Treatment and study plan

no drugs used for this study

Diagnostic Test

tomographic, angiographic and clinical follow up

Primary outcomes

Proportion of subjects with neovascularization at follow-up visit

Time frame: at 5 years of follow up

Evaluation of choroidal neovascularization

Study contacts

Contact information is provided by the study sponsor or research team.

Paolo Milani, MD

CONTACT

[email protected]

+390261911

Sponsors and collaborators

Lead sponsor

Istituto Auxologico Italiano

Other

Registry information

Official study title

Long Term Follow-up of Eyes With High Myopia

Acronym: FWUPMIOPIA_ E

Important dates

Study start: 2023
Primary completion: 2025
Study completion: 2025
First posted: Mar 21, 2024
Registry last updated: May 1, 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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