Norris ORIEN Total Cancer Care

Description

This research trial collects biological samples and clinical information to create a repository of data from patients with cancer or a predisposition for cancer. Combining genetic information from biological samples and clinical data may lead to more knowledge about why certain cancers respond to treatment and help create more personalized medicine.

Conditions

Cancer Risk, Malignant Neoplasm

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Study Overview

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Study Details

Study overview

This research trial collects biological samples and clinical information to create a repository of data from patients with cancer or a predisposition for cancer. Combining genetic information from biological samples and clinical data may lead to more knowledge about why certain cancers respond to treatment and help create more personalized medicine.

Norris ORIEN Total Cancer Care Protocol: A Lifetime Partnership With Patients

Norris ORIEN Total Cancer Care

Condition
Cancer Risk
Intervention / Treatment

-

Contacts and Locations

Los Angeles

USC / Norris Comprehensive Cancer Center, Los Angeles, California, United States, 90033

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Limited to those patients who are registered for outpatient or inpatient care at University of Southern California (USC) Norris
  • * Able to understand and sign the TCCP informed consent, California subject's bill of rights, Health Insurance Portability and Accountability Act (HIPAA), and research authorization form directly or through an authorized representative; the informed consent, subject's bill of rights, HIPAA, and research authorization will be available in both English and Spanish languages
  • * Individuals who are not registered as patients for outpatient or inpatient care at USC Norris
  • * Individuals who are unable to understand or sign the TCCP informed consent, subject's bill of rights, HIPAA, and research authorization in either English or Spanish

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Southern California,

Bodour Salhia, PhD, PRINCIPAL_INVESTIGATOR, University of Southern California

Study Record Dates

2037-05-02