A Study of Tools for Standardizing Clinical Research Metadata Using HL7 FHIR

Overview

About this study

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The overall goal is to design, develop and evaluate an integrated platform for clinical research metadata standardization leveraging both standards-based representation and scalable Semantic Web technologies. The ultimate goal is to advance clinical research data discovery and analytic capabilities for clinical and translational centers and investigators.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria

  • Arm 1
    • Volunteer tester
      • Clinical informatics researchers through research collaboration network
  • Arm 2
    • Ovarian cancer patients
      • Ovarian cancer patients seen in Mayo Clinic and with accessible electronic medical records

Exclusion Criteria

  • Different diagnosed cancers other than ovarian cancer

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Robert Freimuth, Ph.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

International patient clinical studies questions