S1204, Viral Screening in Newly Diagnosed Cancer Patients

Completed

Conditions studied: Cancer

In brief

The goal of this study is to estimate the prevalence of HIV, Hepatitis B and hepatitis C infection among newly diagnosed cancer patients presenting to community and academic oncology clinics.

Key facts

Study ID

NCT01946516

Run by

SWOG Cancer Research Network

People needed

3051

Starts

2013-08-29

Expected to finish

2022-10-13

Last updated by the study team

2023-07-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• presenting for evaluation or treatment of a new cancer malignancy(including hematologic)
• confirmed pathologic diagnosis must be within 120 days of registration (Patients presenting for "second opinions" of confirmed malignancies are eligible, including those who have started cancer treatment at other facilities)
• at least 18 years of age
• patient must have had their blood drawn for HIV, HBV and HCV testing prior to registration (Patients who have had HIV, HBV and/or HCV testing within 60 days prior to registration and who do not wish to be retested are eligible, provided supporting documents can be obtained confirming viral test results for all three viruses. Documentation must be obtained prior to registration.
• Patients who are viral positive for either HIV, HBV, and/or HCV and who do not wish to be retested are eligible, provided documentation of viral load within 120 days prior to registration can be obtained. Note that these patients must be tested for or provide current viral load for all three viruses to be eligible. Documentation must be obtained prior to registration.)
• Patients must sign and give written informed consent in accordance with institutional and federal guidelines
• Patients must be offered the opportunity to allow their blood specimens to be banked by the SWOG Repository for future research

You may not qualify if…

• diagnosed with a malignancy other than the current malignancy within the past five years (with the exception of basal cell or squamous cell skin cancer, in situ cervical cancer, or in situ breast cancer.)

Where it is running

• Kaiser Permanente - Harbor City — Harbor City, California, United States
• Contra Costa Regional Medical Center — Martinez, California, United States
• East Bay Physicians Medical Group-Summit — Oakland, California, United States
• Kaiser Permanente-Oakland — Oakland, California, United States
• Desert Regional Medical Center — Palm Springs, California, United States
• Kaiser Permanente - Panorama City — Panorama City, California, United States
• Kaiser Permanente-Roseville — Roseville, California, United States
• Kaiser Permanente-San Francisco — San Francisco, California, United States
• Kaiser Permanente Medical Center-Vacaville — Vacaville, California, United States
• Kaiser Permanente-Lone Tree — Lone Tree, Colorado, United States
• University of Hawaii Cancer Center — Honolulu, Hawaii, United States
• Tripler Army Medical Center — Honolulu, Hawaii, United States
• Saint Luke's Mountain States Tumor Institute - Meridian — Meridian, Idaho, United States
• Mac Neal Hospital — Berwyn, Illinois, United States
• Weiss Memorial Hospital — Chicago, Illinois, United States
• Hines Veterans Administration Hospital — Hines, Illinois, United States
• West Suburban Medical Center — River Forest, Illinois, United States
• Veteran Administration Eastern Kansas Healthcare — Leavenworth, Kansas, United States
• Topeka VA Hospital — Topeka, Kansas, United States
• LSU Health Baton Rouge-North Clinic — Baton Rouge, Louisiana, United States
• Louisiana Hematology Oncology Associates LLC — Baton Rouge, Louisiana, United States
• Mary Bird Perkins Cancer Center — Baton Rouge, Louisiana, United States
• Medical Oncology LLC — Baton Rouge, Louisiana, United States
• Mary Bird Cancer Center/Saint Tammany Parish — Covington, Louisiana, United States
• Kaiser Permanente Hospital — Fontana, California, United States

Full record on ClinicalTrials.gov

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