A Study to Evaluate the Effectiveness of VIZAMYL™ Reader Training Programme in Europe

NCT04773015 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 227

Last updated 2024-10-10

Study results available
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Summary

This is a study to determine the effectiveness of the VIZAMYL™ reader training programme in clinical practice in Europe

Conditions

Sponsors & Collaborators

  • ICON plc

    collaborator INDUSTRY
  • GE Healthcare

    lead INDUSTRY

Principal Investigators

  • Paul Sherwin, MD, PhD · GE Healthcare

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-12-11
Primary Completion
2021-12-07
Completion
2021-12-07

Countries

  • Austria
  • Finland
  • Italy
  • Netherlands
  • Spain

Study Locations

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Entities

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 NCT04773015 on ClinicalTrials.gov