Behavior and Knowledges of Patients Enrolled Into SIOUX Study

NCT02900586 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2020-03-11

No results posted yet for this study

Summary

The purpose of this study is to contribute to the evaluation of SIOUX study by adding data about the choices of the observant patients, the mis-observant ones or the protocol deviations.

Conditions

Sponsors & Collaborators

  • University of Lorraine

    collaborator OTHER
  • Centre Hospitalier Régional Metz-Thionville

    lead OTHER

Principal Investigators

  • Didier POIVRET, MD · CHR Metz-Thionville

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2017-11-30
Completion
2019-12-31

Countries

  • France

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 NCT02900586 on ClinicalTrials.gov