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Trial record 39 of 56 for:    "Lung Disease" | "Dalteparin"

Weight-Based Enoxaparin Dosing and Real-Time Dose Adjustment in Orthopaedic Trauma

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03339349
Recruitment Status : Recruiting
First Posted : November 13, 2017
Last Update Posted : May 4, 2018
Information provided by (Responsible Party):
University of Utah

Brief Summary:
The rates of Venous thromboembolism (VTE) after orthopedic surgery are as high as 40-60% without prophylactic measures. Enoxaparin, a low-molecular-weight heparin, produces an anticoagulant effect by binding antithrombin, thereby accelerating antithrombin's inactivation of coagulation factor Xa (FXa), thus decreasing the likelihood of clot formation. Despite standard dosing enoxaparin prophylaxis, VTE rates in post-operative orthopedic trauma patients remain as high as 12.2%.The investigators will examine enoxaparin pharmacokinetics and test whether a clinical protocol for real-time enoxaparin dose adjustment can favorably alter the proportion of patients with in-range anti-Factor Xa (aFXa) levels. Outcomes will include peak and trough steady-state aFXa levels in response to standard and escalated doses of enoxaparin and the incidence of venous thromboembolism and bleeding events post-surgery. In the trauma and orthopaedic populations, patients with low initial aFXa levels are significantly more likely to develop deep venous thrombosis. Thus, this study has important implications for appropriate enoxaparin dose magnitude and frequency, and may ultimately help to decrease the substantial morbidity and mortality associated with post-operative VTE.

Condition or disease Intervention/treatment Phase
Venous Thromboembolism Deep Vein Thrombosis Pulmonary Embolus Drug: Enoxaparin Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 137 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Other
Official Title: Weight-Based Enoxaparin Dosing and Real-Time Dose Adjustment in Orthopaedic Trauma
Actual Study Start Date : November 15, 2017
Estimated Primary Completion Date : June 30, 2019
Estimated Study Completion Date : June 30, 2019

Arm Intervention/treatment
Experimental: Enoxaparin Metabolism
Eligible patients will have steady state peak and trough anti-Xa levels drawn after the third enoxaparin dose. For patients in-range (levels 0.2-0.4 IU/mL), no intervention will be undertaken. For patients out of range, enoxaparin dose will be adjusted according to an established dose adjustment algorithm. Repeat levels will be checked after the third administration of the new dose.
Drug: Enoxaparin
Enrolled patients will receive real-time monitoring of peak and trough steady state anti-Xa levels. Out-of-range patients will receive real time dose adjustment of Enoxaparin using a clinical protocol developed with our inpatient pharmacists.

Primary Outcome Measures :
  1. Number of Participants with Venous Thromboembolism Events [ Time Frame: 90 days ]
    Any symptomatic venous thromboembolism events, including deep venous thrombosis or pulmonary embolus occurring within 90 days of surgery

  2. Number of Participants with Bleeding Events [ Time Frame: 90 days ]
    Bleeding events requiring alteration in the course of care within 90 days of surgery

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Receiving orthopedic trauma surgery
  • Able to have enoxaparin initiated within 36 hours after procedure

Exclusion Criteria:

  • Intracranial bleeding/stroke
  • bleeding disorder
  • heparin-induced thrombocytopenia
  • creatinine clearance < 30 mL/minute
  • epidural catheter
  • serum creatinine > 1.6 mg/dL

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03339349

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Contact: Christopher Pannucci, MD 801-581-7719

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United States, Utah
University of Utah Recruiting
Salt Lake City, Utah, United States, 84112
Contact: Christopher J Pannucci, MD, MS         
Sponsors and Collaborators
University of Utah

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Responsible Party: University of Utah Identifier: NCT03339349     History of Changes
Other Study ID Numbers: 102526
First Posted: November 13, 2017    Key Record Dates
Last Update Posted: May 4, 2018
Last Verified: May 2018

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Additional relevant MeSH terms:
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Lung Diseases
Pulmonary Embolism
Venous Thromboembolism
Venous Thrombosis
Embolism and Thrombosis
Vascular Diseases
Cardiovascular Diseases
Respiratory Tract Diseases