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Value of Computertomography-based Autopsy (Virtopsy) Compared With Conventional Autopsy in Patients Dying in Intensive Care Units

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Universitätsklinikum Hamburg-Eppendorf
ClinicalTrials.gov Identifier:
NCT01040520
First received: December 28, 2009
Last updated: February 24, 2012
Last verified: February 2012
  Purpose

The aim of the study is to compare findings generated by computertomography-based autopsy (Virtopsy) with conventional autopsy and clinical diagnoses. Therefore all patients dying while receiving treatment in the Department of Intensive Care Medicine will be undergo virtopsy and, if relatives give informed consent conventional autopsy.


Condition
Autopsy

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Computertomography-based Autopsy (Virtopsy) Versus Conventional Autopsy in Patients Dying in Intensive Care Units

Further study details as provided by Universitätsklinikum Hamburg-Eppendorf:

Enrollment: 284
Study Start Date: January 2010
Study Completion Date: July 2010
Primary Completion Date: July 2010 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

All patients who die while receiving treatment in the Department of Intensive Care Medicine

Criteria

Inclusion Criteria:

  • Patients dying in the Department of Intensive Care Medicine while receiving treatment during the study period

Exclusion Criteria:

  • None
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

No publications provided by Universitätsklinikum Hamburg-Eppendorf

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Universitätsklinikum Hamburg-Eppendorf
ClinicalTrials.gov Identifier: NCT01040520     History of Changes
Other Study ID Numbers: UKE KIM 2010.1
Study First Received: December 28, 2009
Last Updated: February 24, 2012
Health Authority: Germany: Ethics Commission

Keywords provided by Universitätsklinikum Hamburg-Eppendorf:
Compare clinical diagnoses with findings discovered by VIRTOPSY
and conventional autopsy

ClinicalTrials.gov processed this record on November 25, 2014