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

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2008 by University of Parma.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
University of Parma
ClinicalTrials.gov Identifier:
NCT00726570
First received: July 29, 2008
Last updated: August 7, 2008
Last verified: August 2008

July 29, 2008
August 7, 2008
August 2008
May 2009   (final data collection date for primary outcome measure)
Reduction in the area under the curve of maximum amplitude (MA) TEG value over time [ Time Frame: 24 hours from application of SCD ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00726570 on ClinicalTrials.gov Archive Site
  • Reduction in the area under the curve of the r time TEG value over time [ Time Frame: 24 h after application of SCD ] [ Designated as safety issue: No ]
  • Reduction in the area under the curve of the alpha angle TEG value over time [ Time Frame: 24 h after application of SCD ] [ Designated as safety issue: No ]
  • Incidence of hypotension (mean arterial pressure ≤60 mmHg) [ Time Frame: ≤24 h after application of SCD ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Alterations of Blood Clotting With the Use of Sequential Compression Devices on the Lower Limbs
Effects of Sequential Compression Devices on Coagulation Parameters Assessed by TEG® in Patients Undergoing Major Abdominal Surgery

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.

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).

We aim to assess the effects on coagulation when SCD are applied to patients at high risk of DVT in addition to standard LMWH therapy. We 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, we 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).

Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Diagnostic
  • Coagulation, Blood
  • Compression Devices, Intermittent Pneumatic
  • Postoperative Complications
  • Thrombelastography
  • 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
  • Experimental: SCD + LMWH
    This group will receive sequential compression device therapy to the lower limbs from their ICU admission until the morning after surgery.
    Interventions:
    • Device: Sequential compression device therapy
    • Drug: Dalteparin
    • Procedure: TEG
  • Active Comparator: LMWH only
    Patients in this group will receive only standard LMWH therapy during their ICU stay.
    Interventions:
    • Drug: Dalteparin
    • Procedure: TEG

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
40
September 2009
May 2009   (final data collection date for primary outcome measure)

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
Both
18 Years and older
No
Not Provided
Italy
 
NCT00726570
ICU-ICU-01
No
Guido Fanelli, MD, University of Parma
University of Parma
Not Provided
Study Chair: Guido Fanelli, MD University of Parma
Principal Investigator: Maria Barbagallo, MD UO II Anestesia e Rianimazione, Azienda Ospedaliero-Universitaria di Parma
University of Parma
August 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP