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Optical Imaging for Uveal Melanoma patients

Optical Imaging for the follow-up of Uveal Melanoma patients - Optical Imaging for Uveal Melanoma patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57016
Enrollment
30
Registered
2024-04-22
Start date
2025-04-29
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Uveal Melanoma

Interventions

Not applicable.

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Diagnosis of primary uveal melanoma - No history of previous uveal melanoma treatments - No diagnosis of other retinal diseases - Uveal melanoma patients who will be treated with either brachytherapy or proton beam therapy

Exclusion criteria

Exclusion criteria: - Subjects who are not legally capable - Subjects under the age of 18

Design outcomes

Primary

MeasureTime frame
Main study parameters/endpoints: For Ru-106 brachytherapy and PBT treated patients between each timepoint: Primary objective: • Location of FAF changes • Characteristic FAF changes (mottling pattern and rim of increased FAF).

Secondary

MeasureTime frame
Secondary objectives: • For brachytherapy, the diameter of the FAF changes compared to the dimensions of the used applicator. • For PBT, distances of retina with FAF changes to the clip locations. • Relation of FAF changes to abnormalities seen on OCT and funduscopic imaging both at the same timepoint and at later timepoints.

Countries

Netherlands

Contacts

Public ContactI. E. Mulder

Leids Universitair Medisch Centrum

i.e.mulder@lumc.nl071-5296217

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)