The Role of FDG-PET/CT Imaging in the Management of Patients With Thromboembolic Disorders (The PETVET Study)

Sponsor
Odense University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01466426
Collaborator
(none)
40
3
31
13.3
0.4

Study Details

Study Description

Brief Summary

This pilot study aims at validating 18F-flourodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) in the detection and characterization of venous thromboembolism (VTE) in the entire human body, especially deep venous thrombosis (DVT) and pulmonary embolism (PE). On completion of this study the investigators will hopefully be able to demonstrate the importance of functional/molecular imaging technique in managing patients with this common and potentially fatal disorder.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Acute DVT and PE are common and serious conditions. Highly effective treatment (most often anticoagulant agents) is available for acute VTE, but it is associated with potentially dangerous side effects. In addition, DVT and PE are just two manifestations of VTE, which can occur everywhere in the human organism. An underlying disease (i.e. cancer) is often a key factor in developing VTE.

    Commonly used diagnostic imaging techniques in DVT and PE have a fair diagnostic accuracy, but do not address other important aspects of the disease. In contrast to this, FDG-PET/CT has the potential to contribute in VTE diagnosis by

    • Differentiate between acute and chronic VTE

    • Screening of the entire body for VTE (e.g. the pelvis where normal imaging techniques fail)

    • Early diagnosis of underlying disease (e.g. cancer, with the possibility of early treatment)

    This is a pilot study with the above mentioned objectives, and is part of a larger study addressing other aspects of FDG-PET/CT in VTE.

    The investigators believe that their hypothesis that FDG-PET/CT imaging may introduce a new approach for detecting thrombi anywhere in the body, particularly in the venous system including the pelvis and the calves, will add a new dimension in treating patients with suspected PE. This technology will only detect acute thrombi and not chronic thrombi that no longer have activity, which will obviate unnecessary treatment in this population.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    40 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    The Role of FDG-PET/CT Imaging in the Management of Patients With Thromboembolic Disorders
    Study Start Date :
    Nov 1, 2011
    Actual Primary Completion Date :
    Dec 1, 2013
    Actual Study Completion Date :
    Jun 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    DVT confirmed

    DVT ruled out

    PE confirmed

    PE ruled out

    Outcome Measures

    Primary Outcome Measures

    1. Proof-of-concept [During diagnostic workup]

      Simple assessment of scans - positive or negative in the relevant patient categories

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Positive or negative diagnosis of VTE (DVT/PE)

    • Age ≥ 50 years

    • Informed consent obtained

    • Symptoms < 1 week

    Exclusion Criteria:
    • Pregnant or lactating women

    • Foreign language patients with a need for an interpreter

    • Previous DVT or PE

    • Known malignancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dept. of Acute Medicine, Odense University Hospital Odense Denmark dk-5000
    2 Dept. of Nuclear Medicine, Odense University Hospital Odense Denmark dk-5000
    3 Dept. of Respiratory Medicine, Odense University Hospital, Odense Denmark dk-5000

    Sponsors and Collaborators

    • Odense University Hospital

    Investigators

    • Study Chair: Soeren Hess, MD, Odense University Hospital
    • Study Chair: Poul Henning Madsen, MD, Odense University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Søren Hess, MD, MD, Odense University Hospital
    ClinicalTrials.gov Identifier:
    NCT01466426
    Other Study ID Numbers:
    • NMA projekt K 59 PETVET
    First Posted:
    Nov 8, 2011
    Last Update Posted:
    Oct 28, 2014
    Last Verified:
    Oct 1, 2014
    Keywords provided by Søren Hess, MD, MD, Odense University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 28, 2014