MedTrace Logo

Multi-site Decision Impact Study for Decipher

NCT02034825 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2016-02-29

No results posted yet for this study

Summary

This prospectively designed retrospective clinical utility study will evaluate urologists' treatment recommendations before and after reviewing Decipher results for selected patient cases.

Conditions

Interventions

OTHER

Decipher Questionnaire

Each participant will complete the pre and post-Decipher eCRQs for a minimum of 5 cases, and a maximum of 25 cases.

Sponsors & Collaborators

Principal Investigators

  • Badani K Ketan, MD · Columbia University

  • Christine d Buerki, PhD · GenomeDx Biosciences Inc.

  • Vipul Patel, MD · AdventHealth

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2015-01-31
Completion
2015-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02034825 on ClinicalTrials.gov