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Clinical Trials/NCT01649453
NCT01649453
Terminated
Not Applicable

A Prospective Study of Clinical Outcomes for the Pathwork® Tissue of Origin Test

Cedar Associates LLC1 site in 1 country19 target enrollmentMay 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neoplasm Metastasis
Sponsor
Cedar Associates LLC
Enrollment
19
Locations
1
Primary Endpoint
Survival
Status
Terminated
Last Updated
13 years ago

Overview

Brief Summary

The study prospectively assesses the change in cancer-specific clinical decisions and outcomes before and after physicians received results from the Pathwork® Tissue of Origin (TOO) Test for patients whose primary site of cancer origin is uncertain.

Registry
clinicaltrials.gov
Start Date
May 2012
End Date
February 2013
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Cedar Associates LLC
Responsible Party
Principal Investigator
Principal Investigator

John Hornberger, MD MS

CEO, President

Cedar Associates LLC

Eligibility Criteria

Inclusion Criteria

  • their physician ordered or intends to order a Pathwork® TOO Test between May 2012 and December 2013
  • the patient is ≥ 18 years of age
  • the patient has given informed consent (online or verbal)
  • the patient is able to understand English.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Survival

Time Frame: 2 years

Study Sites (1)

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