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NCT04588662Active, not recruiting

A Prospective Natural History Study in Uveal Melanoma

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Brief summary (registry, in English)

The overall objective of this proposal is to develop and utilize a multicenter UM registry that will, in a longitudinal fashion, capture prospective data in order to characterize the natural history of UM and provide data that will be used to support the development of novel therapies for this disease. The care of patients with UM requires a multi-disciplinary team of physicians that commonly requires the involvement of both radiation oncology and interventional radiology, and is typically directed by an ophthalmologic oncologist at time of initial diagnosis of primary disease. Overall management is transitioned to a medical oncologist when distant recurrence is identified. In the case that a patient presents with metastasis at the time of diagnosis, a medical oncologist typically directs overall management. The management of surveillance for the development of metastasis following the treatment of primary disease is variable and, if performed at all, is managed by either an ophthalmologic oncologist or medical oncologist. Thus, the successful development of a registry that aims to capture the data regarding the full natural history of UM requires a collaborative effort including leaders from both the UM ophthalmologic oncology and medical oncology fields. To this end, the investigators have built an initial consortium of key ophthalmologic oncology and medical oncology leaders from multiple major UM centers in the United States.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
122 (actual)
First submitted
16 Jul 2020
Start date
6 May 2021
Primary completion date
Mar 2027
Lead sponsor
Columbia University
Diseases
Melanoma
NCT number
NCT04588662

What you commit to

  • Study type: Observational
  • Participants enrolled: 122
  • From 6 May 2021 to the primary completion date, Mar 2027
  • 17 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \*None

Who the study is looking for

  • Diagnosis of uveal melanoma
  • Ability to provide written informed consent for participation in the prospective registry OR an institutional waiver by the IRB/ethics committee for retrospective data collection without written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (17)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Royal Adelaide Hospital
Coordinator of this site? Confirm its status
AdelaideAustraliaUnknown status
Chatswood Eye Specialists
Coordinator of this site? Confirm its status
ChatswoodAustraliaUnknown status
Royal Victorian Eve and Ear Hospital
Coordinator of this site? Confirm its status
East MelbourneAustraliaUnknown status
Western Eye Specialists
Coordinator of this site? Confirm its status
MaribyrnongAustraliaUnknown status
Pennington Eye Clinic
Coordinator of this site? Confirm its status
North AdelaideAustraliaUnknown status
Perth Retina
Coordinator of this site? Confirm its status
SubiacoAustraliaUnknown status
Dr. Conway Private Rooms
Coordinator of this site? Confirm its status
SydneyAustraliaUnknown status
St Vincent's Hospital
Coordinator of this site? Confirm its status
SydneyAustraliaUnknown status
Princess Margaret Cancer Center
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Erlangen
Coordinator of this site? Confirm its status
ErlangenGermanyUnknown status
Clatterbridge Cancer Centre
Coordinator of this site? Confirm its status
BirkenheadUnited KingdomUnknown status
Mount Vernon Cancer Centre
Coordinator of this site? Confirm its status
NorthwoodUnited KingdomUnknown status
Sheffield
Coordinator of this site? Confirm its status
SheffieldUnited KingdomUnknown status
Massachusetts General Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
MD Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Thomas Jefferson University Hospital
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.