Autopsy and Photon Counting Computed Tomography to Evaluate Thromboses Related to Central Venous Catheters

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThomas Kander

About this trial

Central venous (CVC) is essential in modern healthcare but unfortunately associated with complications, including thrombosis. In a recently published study, it was showed that 12 out of 12 deceased patients had subclinical CVK-related thrombosis (Rockholt et al.). To shed light on this problem, the current studies were designed. In sub-study 1, deceased patients with CVC who are referred for clinical autopsy are included. Before the autopsy, the deceased will be examined with a photon-counting computed tomography (CT) scan and the results will be compared.

In sub-study 2, living patients with CVC who are referred for various CT scans without contrast, are included. After informed consent, the patient will be examined with the photon-counting CT, whose reliability has been validated in Part 1 and the incidence of subclinical CVC-related thrombosis will be reported.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diseased patients with an indwelling central venous catheter and a clinical indication for autopsy

Informed and signed consent from next of kind

Disqualifiers

None

Living patients with an indwelling central venous catheter who are referred to a CT scan without iv contrast

Informed and signed consent from the patient

Trial population

Substudy 1: Diseased patients with an indwelling central venous catheter and a clinical indication for autopsy Substudy 2: Living patients with an indwelling central venous catheter who are referred to a CT scan without iv contrast

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Diseased patients with an indwelling central venous catheter who is referred to autopsy

    Diagnostic test

    Photon counting CT is performed and the results are compared to the results of the autopsy

  • Living patients with an indwelling central venous catheter referred to a CT scan without iv contrast

    Radiation

    Patients will be investigated using a photon counting CT. Prior to the investigation patients will be investigated with ultrasound. The results from the two modalities will be compared

Treatment groups

75 Participants
are divided into 2 treatment groups
Group A: Diseased patients with an indwelling central venous catheter1 intervention
Group B: Living patients with an indwelling central venous catheter1 intervention

Trial outcomes

Primary outcomes

1

The incidence of venous thrombosis related to a central venous catheter in diseased patients

Venous thrombosis related to a central venous catheter detected at autopsy

Time frame
At autopsy
2

The performance of the photon counting CT on diseased patients

The performance of the photon counting CT will be evaluated by comparing the findings from the CT with the findings from the autopsy

Time frame
After death. The CT scan and the autopsy will be performed within 1 week after death
3

The incidence of venous thrombosis related to a central venous catheter in living patients

The incidence of venous thrombosis related to a central venous catheter in living patients detected with a photon counting CT

Time frame
At CT scan
4

The performance of ultrasound compared to the photon counting CT

The performance of ultrasound compared to the photon counting CT in detecting enous thrombosis related to central venous catheters

Time frame
Ultrasound will be performed ±24 hours from the CT

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Thomas Kander

Lead sponsor

Region Skane

Sponsor institution