Nashville, Tennessee 37203


This is an investigational multi-site outcomes registry intended to collect information about a patient's cancer care. Patients may enter the Registry at any time during the patient's current stage in the continuum of care. The registries main objectives will be to measure and evaluate the effects of patient care throughout the care continuum, resulting in the identification of the most effective treatment options. Objectives will encompass evaluations and analytics around safety, effectiveness, and improved efficiencies.

Study summary:



Inclusion Criteria: - 18 or older - Patients that have been diagnosed with/ or are thought to have any form of cancer at any stage in the continuum of their care from screening through survivorship. - Patient must have the ability to understand the nature of the trial and give written informed consent Exclusion Criteria: - There are no exclusion criteria for this Outcomes Registry



Primary Contact:

Principal Investigator
Richard Geer, MD
Sarah Cannon

Catherine Howard

Backup Contact:


Location Contact:

Nashville, Tennessee 37203
United States

Catherine Howard

Site Status: Recruiting

Data Source:

Date Processed: March 16, 2018

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