TEGLeg: Alterations of Blood Clotting With the Use of Sequential Compression Devices on the Lower Limbs

Sponsor
University of Parma (Other)
Overall Status
Terminated
CT.gov ID
NCT00726570
Collaborator
(none)
40
1
2
27
1.5

Study Details

Study Description

Brief Summary

This study aims to assess possible alteration in coagulation (blood clotting) following treatment with sequential compression devices (SCD) plus low-molecular weight heparin (LMWH) as opposed to LMWH alone.

The investigators will examine coagulation in the early postoperative period of patients undergoing major abdominal surgery during their stay in our Intensive Care Unit.

In addition to common laboratory tests, the investigators will examine coagulation using TEG®, a device which allows a semi-quantitative examination of all phases of coagulation.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Low molecular weight heparins (LMWH) are routinely used in perioperative prophylaxis of thromboembolic complications [(chiefly deep vein thrombosis (DVT)]. LMWHs have been proved to be safe and equipotent or superior when compared with unfractionated heparin.

Sequential compressing devices (SCD) are relatively novel pneumatic stockings with several air chambers. A computerized pump applies a gradient of pressure which decreases from the foot cranially. Pressure is also applied intermittently according to predetermined schedules. This devices are being employed for DVT prophylaxis in patients for whom anticoagulation therapy is contraindicated, or in those who have a low risk of DVT. They have also been employed to complement anticoagulant therapy in patients at high risk of DVT, such as those undergoing orthopedic surgery (Fordyce, 1992; Handoll, 2002; Warwick, 2002; Pitto, 2004).

The mechanism of action of SCD seems to be primarily mechanical, through a displacement of a column of blood through the venous system and towards the heart; they act as a surrogate of the muscular pump in immobilized patients (Killewich, 1995).

There is also some evidence that SCD activity may influence the coagulation/fibrinolysis system towards hypocoagulability (Dai, 2000; Kohro, 2003); Kohro and colleagues have also hypothesized that the shear forces generated by SCD may alter platelet adhesion by a direct effect on platelets and/or by increasing the release of factors from the venous endothelium (Kohro, 2005).

The investigators aim to assess the effects on coagulation when SCD are applied to patients at high risk of DVT in addition to standard LMWH therapy.The investigators chose to study a population in whom SCD may be useful in reducing the incidence of DVT, such as patients undergoing postoperative monitoring in the intensive care unit (ICU) after major abdominal surgery for cancer.

In addition to standard laboratory tests, the investigators will use thrombelastography (TEG®) to assess all phases of coagulation. A TEG parameter, maximum amplitude (MA), has been linked to an increase of thrombotic complications in a postoperative population (McCrath, 2005).

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Effects of Sequential Compression Devices on Coagulation Parameters Assessed by TEG® in Patients Undergoing Major Abdominal Surgery
Study Start Date :
Aug 1, 2008
Actual Primary Completion Date :
Nov 1, 2010
Actual Study Completion Date :
Nov 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: SCD + LMWH

This group will receive sequential compression device therapy to the lower limbs from their ICU admission until the morning after surgery.

Device: Sequential compression device therapy
Pneumatic stockings will be applied to patients. Pressures ranging from 12 to 40 mmHg will be applied at different levels of the lower limb for 40-second cycles at 2-minute intervals. Therapy will continue until the morning after surgery.
Other Names:
  • SCD EXPRESS
  • Foot pump
  • Drug: Dalteparin
    2500 UI qd if ≤ 50 kg body weight 5000 UI qd if > 50 kg
    Other Names:
  • low molecular weight heparin
  • Fragmin
  • heparin
  • thromboprophylaxis
  • anticoagulant
  • LMWH
  • Procedure: TEG
    A 2-ml blood sample will be used for each exam. A full analysis will be run both with and without heparinase at each time point. TEG analyses will be run at: Patient admission (before SCD start) 40-60 min after admission Morning after surgery
    Other Names:
  • thrombelastography
  • TEG®
  • thrombelastogram
  • Active Comparator: LMWH only

    Patients in this group will receive only standard LMWH therapy during their ICU stay.

    Drug: Dalteparin
    2500 UI qd if ≤ 50 kg body weight 5000 UI qd if > 50 kg
    Other Names:
  • low molecular weight heparin
  • Fragmin
  • heparin
  • thromboprophylaxis
  • anticoagulant
  • LMWH
  • Procedure: TEG
    A 2-ml blood sample will be used for each exam. A full analysis will be run both with and without heparinase at each time point. TEG analyses will be run at: Patient admission (before SCD start) 40-60 min after admission Morning after surgery
    Other Names:
  • thrombelastography
  • TEG®
  • thrombelastogram
  • Outcome Measures

    Primary Outcome Measures

    1. Reduction in the area under the curve of maximum amplitude (MA) TEG value over time [24 hours from application of SCD]

    Secondary Outcome Measures

    1. Reduction in the area under the curve of the r time TEG value over time [24 h after application of SCD]

    2. Reduction in the area under the curve of the alpha angle TEG value over time [24 h after application of SCD]

    3. Incidence of hypotension (mean arterial pressure ≤60 mmHg) [≤24 h after application of SCD]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Elective major abdominal surgery for neoplasm

    • Planned admission to postsurgical ICU due to the patient's meeting one or more of the following:

    • ASA Physical Status Class 4

    • Surgery of modified Johns-Hopkins class ≥IV

    • ASA 3 with modified Johns-Hopkins class 3 surgery

    • Expected duration of surgery ≥8 h

    Exclusion Criteria:
    • History of coagulation abnormalities, either congenital or acquired

    • Ongoing treatment with anticoagulants/antiplatelet agents other than LMWH or hormones

    • Massive edema of the legs

    • Severe peripheral arteriopathy or neuropathy

    • Malformations or recent surgery/trauma to the lower extremities

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital / Azienda Ospedaliero-Universitaria Parma PR Italy 43100

    Sponsors and Collaborators

    • University of Parma

    Investigators

    • Study Chair: Guido Fanelli, MD, University of Parma
    • Principal Investigator: Maria Barbagallo, MD, UO II Anestesia e Rianimazione, Azienda Ospedaliero-Universitaria di Parma

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Guido Fanelli, MD, University of Parma
    ClinicalTrials.gov Identifier:
    NCT00726570
    Other Study ID Numbers:
    • ICU-ICU-01
    First Posted:
    Aug 1, 2008
    Last Update Posted:
    Nov 5, 2013
    Last Verified:
    Nov 1, 2013

    Study Results

    No Results Posted as of Nov 5, 2013