A Feasibility Study of Virtopsy With Tissue Sampling in Besancon University Hospital

NCT03877900 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2020-10-05

No results posted yet for this study

Summary

The aim of this project is to assess the feasibility of a new local post mortem procedure at Besançon University Hospital : Virtopsy+, magnetic resonance (MR) imaging with tissue sampling of the fetus and newborns.

Conditions

  • Stillbirth and Fetal Death
  • Termination of Pregnancy
  • Neonatal Death

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Besancon

    lead OTHER

Principal Investigators

  • Marion AUBER LENOIR, MD · CHU Besançon

Eligibility

Max Age
1 Month
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-28
Primary Completion
2020-03-06
Completion
2020-03-06

Countries

  • France

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 NCT03877900 on ClinicalTrials.gov