Structural Orbital Changes in Anophthalmic Socket Syndrome

Universitaire Ziekenhuizen KU Leuven

Status: Completed

Conditions: Anophthalmic Socket Syndrome; Anophthalmos; Acquired

Treatments: Diagnostic Test: MRI

Study type: Interventional

Funder types: Other

Identifiers

NCT04395404

s62697

Details and patient eligibility

About

Understand better the aetiology and physiopathogenesis of anophthalmic socket syndrome.

Enrollment: 10 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 18 years or older
• Unilateral anophthalmic socket syndrome (superior sulcus grading 0 till 4)
• Enucleation/evisceration with primary implant more than 5 years ago
• After informed consent

Exclusion criteria

• MRI absolute and relative contraindications such as metallic fragments or metallic containing devices,
• history of orbital trauma, previous anophthalmic socket and eyelid surgery, inflammation, infection, buphthalmos, congenital anophthalmos and radiation

Trial design

Primary purpose: Basic Science

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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10 participants in 1 patient group

Single arm

Experimental group

Treatment:

Diagnostic Test: MRI