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ThromboembolismNCT01541995

Evaluation of Contrast Medium Enhanced Post-mortem CT in Virtual Autopsy

An observational study of Thromboembolism and Vascular Conditions, run by Universitätsklinikum Hamburg-Eppendorf at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study aims to compare the value of contrast medium enhanced post mortem CT to classic autopsy. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Thromboembolism, Vascular Conditions
How many people
50 participants
Where
1 siteGermany
Study dates
Apr 2012to Aug 2013
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: patients dying in the ICU during the study period

Who may be able to join

  • Patients dying in the ICU
  • age >18y

Who cannot join

  • relatives refusing to participation in the study

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • University Medical Center Hamburg-Eppendorf

    Hamburg, Free and Hanseatic City of Hamburg, 20246

Other trials in Germany

About this study

The study aims to compare the value of contrast medium enhanced post mortem CT to classic autopsy.

Keywords
contrast medium enhanced post mortem CT, virtual autopsy, To evaluate the value of contrast medium enhanced post-mortem CT in virtual autopsy focussing on thromboembolic and vascular conditions
Medical subject headings
Thromboembolism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01541995
Study groupRoleWhat they receive
virtual and classic autopsyPatients where contrast medium enhanced post mortem CT and classic autopsy will be performed.
virtual autopsy onlyPatients where only contrast medium enhanced post mortem CT will be performed.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Mar 2012 (estimated)
  2. Study startApr 2012
  3. Primary completionAug 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01541995
Sponsor's protocol ID
VA-3 Contrast Medium
Status last verified
Sep 2013
First submitted
24 Feb 2012
Last updated
30 Sep 2013
Results posted
No
Data monitoring committee
No

Publications

  • Wichmann D, Heinemann A, Weinberg C, Vogel H, Hoepker WW, Grabherr S, Pueschel K, Kluge S. Virtual autopsy with multiphase postmortem computed tomographic angiography versus traditional medical autopsy to investigate unexpected deaths of hospitalized patients: a cohort study. Ann Intern Med. 2014 Apr 15;160(8):534-41. doi: 10.7326/M13-2211.

    PubMed 24733194

Questions about this trial

What is this clinical trial studying?

An observational study of Thromboembolism and Vascular Conditions, run by Universitätsklinikum Hamburg-Eppendorf at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Sep 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01541995, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Sep 2013; AzTrials last refreshed its copy on 1 Nov 2026.

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