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Developing and Testing a Personalized Evidence-based Shared Decision-making Tool for Stent Selection

NCT02046902 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 586

Last updated 2019-08-06

Study results available
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Summary

The goal of this study is to gather input from patients who have undergone PCI, their family and/or caregivers, and clinicians to develop a patient decision aid. The purpose of the decision aid is to deliver information, including individualized estimates of patients' restenosis risk, in an understandable format that would be informative and assist in decision-making for patients undergoing PCI.

Conditions

  • Heart Diseases

Sponsors & Collaborators

  • Patient-Centered Outcomes Research Institute

    collaborator OTHER

  • University of Missouri, Kansas City

    lead OTHER

Principal Investigators

  • John A Spertus, MD, MPH · University of Missouri, Kansas City

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • United States

Study Locations

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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 NCT02046902 on ClinicalTrials.gov