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
John Hornberger, MD MS
CEO, President
Cedar Associates LLC
Study Sites (1)
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