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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00351728
Other study ID # UCLA IRB #05-04-016
Secondary ID
Status Completed
Phase N/A
First received July 12, 2006
Last updated July 5, 2016
Start date June 2006
Est. completion date August 2012

Study information

Verified date July 2016
Source Jonsson Comprehensive Cancer Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Patients diagnosed with ocular melanoma consent to participate in the study. Combined PET/CT scans of the whole body are performed at baseline, three months later, and six months after that for a total of three combined scans in the first year. Subsequently, these combined scans will be performed at 6-monthly intervals for a total of two combined scans per year.


Recruitment information / eligibility

Status Completed
Enrollment 174
Est. completion date August 2012
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Patients with a diagnosis of ocular melanoma (a pigmented malignant tumor) involving the choroid and/or ciliary body (the blood vessel layer in the back of the eye and/or the part of the eye behind the iris).

2. Patients 18 years of age or older.

3. Patients able to give informed consent.

Exclusion Criteria:

1. Patients who refuse to participate in the study.

2. Patients who are unable to cooperate with or cannot undergo PET/CT scanning.

3. Patients who will be moving out of the area of UCLA during the ten years of this study.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Jules Stein Eye Institute Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
Jonsson Comprehensive Cancer Center

Country where clinical trial is conducted

United States, 

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