POPLITEA: Deep Venous Thrombosis After Hepatobiliopancreatic Surgery

Sponsor
Technische Universität Dresden (Other)
Overall Status
Terminated
CT.gov ID
NCT02649023
Collaborator
(none)
76
1
27
2.8

Study Details

Study Description

Brief Summary

To investigate the incidence of pre- and early postoperative deep venous thrombosis in patients undergoing hepatobiliopancreatic surgery, as well as potential corresponding risk factors with special attention to circulating tumor cells.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Thromboembolic events are a common cause of morbidity and mortality in oncological patients. Up to 20% of cancer patients suffer from venous thromboembolism (VTE) induced by the underlying malignancy itself. Oncologic gastrointestinal surgery is a well-known risk factor for VTE. About 4-6% of patients undergoing elective hepatobiliopanreatic surgery develop a deep venous thrombosis (DVT) or pulmonary embolism. However, there are no data referring to the incidence of DVT shortly ahead of the surgical event, implementing that a certain percentage of postoperative DVT might have already been acquired before the operation. Furthermore, most studies only evaluate the rate of symptomatic VTE. In this study, all patients undergoing hepatobiliopancreatic surgery will be screened for deep venous thrombosis the day before surgery, on the third postoperative day (primary endpoint) and 90 days after the operation with a 2-point compression sonography of the lower extremities. The development of a symptomatic VTE (DVT or pulmonary embolism) will be recorded as secondary endpoint. Risk factors, perioperative morbidity / mortality and presence of circulating tumor cells will be analyzed with regard to VTE incidence.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    76 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Pre- and Early Postoperative Deep Venous Thrombosis in Patients Undergoing Oncological Hepatic or Panreatic Resection
    Study Start Date :
    Jan 1, 2016
    Actual Primary Completion Date :
    Apr 1, 2018
    Actual Study Completion Date :
    Apr 1, 2018

    Arms and Interventions

    Arm Intervention/Treatment
    A: Patients with deep venous thrombosis

    All patients will be screened for deep venous thrombosis on postoperative day 3. Patients with a positive finding will be grouped in arm "A"

    B: Patients without deep venous thrombosis

    All patients will be screened for deep venous thrombosis on postoperative day 3. Patients with a negative finding will be grouped in arm "B"

    Outcome Measures

    Primary Outcome Measures

    1. Deep venous thrombosis on day 3 after surgery [3 days]

      Patients will be screened for deep venous thrombosis using a compression ultrasonography at the popliteal and common femoral vein. In case of a pathological finding, a complete compression duplex sonography of the lower extremities will be used for specification.

    Secondary Outcome Measures

    1. Symptomatic deep venous thrombosis or pulmonary embolism during hospital stay [30 days]

      Patients who develop clinical signs of a DVT like swelling of the leg, pain or tenderness in the leg, increased warmth, red or discolored skin of the leg, will be diagnosed by complete compression duplex sonography for confirmation of a deep venous thrombosis. Patients who develop clinical signs of pulmonary embolism like unexplained shortness of breath, pain with deep breathing, coughing of blood, chest pain with electrocardiographic signs of right ventricular stress will be diagnosed by CT pulmonary angiography for confirmation of central or peripheral pulmonary embolism.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients scheduled for elective oncological liver or pancreatic resection

    • Age equal or greater than 18 years

    • Written informed consent

    Exclusion Criteria:
    • Preexistent coagulopathy

    • History of previous VTE

    • benign disease

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of GI, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, TU Dresden Germany 01307

    Sponsors and Collaborators

    • Technische Universität Dresden

    Investigators

    • Principal Investigator: Nuh Rahbari, MD, Department of GI, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, TU Dresden

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Technische Universität Dresden
    ClinicalTrials.gov Identifier:
    NCT02649023
    Other Study ID Numbers:
    • VTG-05
    First Posted:
    Jan 7, 2016
    Last Update Posted:
    Mar 15, 2019
    Last Verified:
    Mar 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 15, 2019