- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00344799
Cytogenetic Study of Ocular Melanoma
March 25, 2021 updated by: Jonsson Comprehensive Cancer Center
Molecular and Cytogenetic Studies of Ocular Melanoma
Patients who are diagnosed with choroidal melanoma and undergo I-125 plaque or enucleation surgery consent to participate in the study.
A tumor sample taken during surgery is studied in the lab for genetic features.
These features and features of subjects' clinical course are recorded.
Analysis of the data may identify genetic features that are indicative of prognostic factors including risk of metastasis.
Study Overview
Status
Completed
Conditions
Detailed Description
The Jules Stein Eye Institute Ocular Melanoma Research Group is conducting cytogenetic studies of choroidal melanoma to improve the screening of biopsy samples of choroidal melanoma through cytogenetic analysis.
Our goal is to identify molecular probes that specifically target regions of chromosomes that undergo changes characteristic of metastatic choroidal melanoma.
Study Type
Observational
Enrollment (Actual)
95
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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California
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Los Angeles, California, United States, 90095
- Jules Stein Eye Institute
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients who have been diagnosed with ocular melanoma, and underwent melanoma treatment at our facility.
Description
Inclusion Criteria:
- Patient with diagnosis of ocular melanoma
- Patient with local treatment plan for ocular melanoma- plaque brachytherapy or enucleation
- Patient 18 years of age or older
- Archival enucleation specimens with diagnosis of ocular melanoma
Exclusion Criteria:
- Patient who refuses local melanoma treatment
- Patient who refuses to participate in this study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Tara M McCannel, MD, PhD, Jules Stein Eye Institute, UCLA
- Study Director: Bradley R Straatsma, MD, JD, Jules Stein Eye Institute, UCLA
- Study Chair: Lynn Gordon, MD, PhD, Jules Stein Eye Institute, UCLA
- Study Chair: Ben Glasgow, MD, Jules Stein Eye Institute, UCLA
- Study Chair: Nagesh P Rao, PhD, UCLA Pathology and Laboratory Medicine
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
January 8, 2005
Primary Completion (ACTUAL)
October 23, 2020
Study Completion (ACTUAL)
October 23, 2020
Study Registration Dates
First Submitted
June 26, 2006
First Submitted That Met QC Criteria
June 26, 2006
First Posted (ESTIMATE)
June 27, 2006
Study Record Updates
Last Update Posted (ACTUAL)
March 29, 2021
Last Update Submitted That Met QC Criteria
March 25, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UCLA IRB#04-12-084
- 11-000847 (OTHER: University of California at Los Angeles)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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