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Longitudinal Follow-Up of Patients Treated With Hypofractionated Stereotactic Photon Radiotherapy Due to Uveal Melanoma

Longitudinal Follow-Up of Retinopathy and Opticopathy After Treatment With Hypofractionated Stereotactic Photon Radiotherapy Due to Uveal Melanoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06280040
Enrollment
20
Registered
2024-02-28
Start date
2023-11-23
Completion date
2025-06-30
Last updated
2024-03-06

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

Conditions

Uveal Melanoma

Brief summary

The purpose of this study is to evaluate the incidence and severity of retinopathy and opticopathy one year after treatment with hypofractionated stereotactic photon radiotherapy due to uveal melanoma. Patients will be imaged before radiation, as well as 3, 6, 9 and 12 months after radiation using sonography funds photography, optical coherence tomography angiography, oximeter and microperimetry.

Interventions

DIAGNOSTIC_TESTClinical examination and multimodal ocular imaging

Imaging consists of sonography, fundus photography, oximeter, optical coherence tomography angiography, and Microperimetry.

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with newly diagnosed uveal melanoma, who will be treated with hypofractionated stereotactic photon radiotherapy as part of clinical routine.

Exclusion criteria

* unwillingness to participate in the study * severe media opacity

Design outcomes

Primary

MeasureTime frameDescription
Incidence and Severity of Retinopathy1 yearIncidence and severity of retinopathy will be evaluated as non-perfusion areas on optical coherence tomography angiography

Secondary

MeasureTime frameDescription
Incidence and Severity of Opticopathy1 yearIncidence and severity of retinopathy will be evaluated on clinical examination and fundus photography
Functional Outcome1 yearFunctional outcome will be evaluated as mean retinal sensitivity.
Incidence and Severity of Retinopathy and Opticopathy in oximeter1 yearIncidence and severity of retinopathy and opticopathy will be evaluated using oxygen saturation

Countries

Austria

Contacts

Primary ContactJudith Kreminger, MD
judith.kreminger@meduniwien.ac.at0043 1 40400 48470
Backup ContactReinhard Told, MD, PhD
reinhard.told@meduniwien.ac.at0043 1 40400 48470

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026