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Clinical Trials/NCT01649453
NCT01649453TerminatedNot Applicable

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

Cedar Associates LLC1 site in 1 country19 target enrollmentStarted: May 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
19
Locations
1
Primary Endpoint
Survival

Study 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.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Cedar Associates LLC
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

John Hornberger, MD MS

CEO, President

Cedar Associates LLC

Study Sites (1)

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