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Optimal Duration of Anticoagulation in Deep Venous Thrombosis (MORGAGNI)

Primary Purpose

Deep Vein Thrombosis of Lower Limb, Lower Extremity Deep Venous Thrombosis Recurrent

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Sodium warfarin
Sponsored by
University of Padova
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Deep Vein Thrombosis of Lower Limb focused on measuring Deep venous thrombosis, Pulmonary embolism, Ultrasonography, D-dimer, Venous thromboembolism, Bleeding

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with proximal DVT that is idiopathic or secondary to minor factors for thrombosis, with or without contemporary manifestations of PE, who have completed an uneventful 3 to 24-month period of anticoagulation and are available for an overall 48-month follow-up at the study centre.

Exclusion Criteria:

  • previous thromboembolism
  • recent (less than 3 months) major trauma or surgery
  • active cancer
  • immobilization resulting from chronic irreversible medical diseases
  • need for indefinite anticoagulation for medical reasons other than VTE
  • impossibility to attend the follow-up visits or to have D-dimer determinations
  • already known major thrombophilia: carriage of deficiencies of natural anticoagulants, lupus-like anticoagulants, homozygosis for factor V Leiden or prothrombin mutation, heterozygosis for both abnormalities
  • short (less than 1 year) life expectancy
  • pregnancy
  • age younger than 18
  • refusal of informed consent

Sites / Locations

  • Paolo Prandoni

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Proximal DVT

Arm Description

Patients whose veins have recanalized (either at the recruitment or later on during the follow-up) will receive the D-dimer determination before discontinuing sodium warfarin. Veins are defined as recanalized when the vein diameter under maximum compressibility is lower than 4 mm both at the common femoral and at the popliteal vein. In those with negative D-dimer sodium warfarin will be discontinued. These patients will have two further determinations of D-dimer (after 1 and 3 months, respectively). While patients with persistently negative D-dimer will no longer receive sodium warfarin, those in whom D-dimer is positive or reverts to positive values in the following determinations will have their sodium warfarin resumed and no longer discontinued.

Outcomes

Primary Outcome Measures

Recurrent venous thromboembolism (VTE)
To assess the rate of recurrent symptomatic VTE (expressed as rate/1000 patients-yeas) occurring after discontinuation of oral anticoagulant therapy up to the study conclusion.

Secondary Outcome Measures

Development of major bleeding complications
To assess the rate of major or clinically relevant bleeding complications (expressed as rate/1000 patients-years) occurring during oral anticoagilant therapy up to the study conclusion

Full Information

First Posted
April 30, 2010
Last Updated
July 17, 2016
Sponsor
University of Padova
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1. Study Identification

Unique Protocol Identification Number
NCT01285661
Brief Title
Optimal Duration of Anticoagulation in Deep Venous Thrombosis
Acronym
MORGAGNI
Official Title
Identification of the Optimal Duration of Anticoagulation in Patients With Deep Venous Thrombosis of the Lower Extremities With the Use of Residual Vein Thrombosis in Combination With D-Dimer
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
March 2010 (undefined)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Padova

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Prospective cohort study aimed at optimizing the duration of anticoagulant treatment in patients at their first episode of proximal deep venous thrombosis (DVT) of the lower extremities, whose pathogenesis is either unknown (idiopathic DVT) or associated with minimal risk factors for thrombosis, with the help of an algorithm which incorporates both ultrasonography and D-dimer information. All patients will be followed-up until 1) the achievement of a major end-point; 2) the date of lost to to followup; 3) the date of death; 4) the date of study stop. The purpose of this study is to demonstrate the safety of withholding anticoagulation from a subgroup of patients with proximal DVT whose veins have recanalized and present with a repeatedly negative D-dimer (at baseline, after 1 and 3 months). The approach will be deemed to be safe if the annual rate of recurrent VTE in patients who will have their anticoagulation discontinued is lower than 5%.
Detailed Description
After giving informed consent, patients will receive an ultrasound investigation of the proximal-vein system (common femoral vein at groin, popliteal vein up to its trifurcation): Patients with residual thrombosis (defined as a diameter of at least 4 mm in at least one spot) will have their anticoagulation continued. A repeat ultrasound is scheduled after 6, 12, 18, 24 and 36 months. In patients with persistently residual thrombosis anticoagulation will not be discontinued, while those whose veins have recanalized will have a decision making process based on the behaviour of D-dimer (see below). Patients whose veins have recanalized (either at the recruitment or later on) will receive the D-dimer determination before discontinuing anticoagulation. In those with negative D-dimer anticoagulation will be discontinued. These patients will have two further determinations of D-dimer (after 1 and 3 months, respectively). While patients with persistently negative D-dimer will no longer receive anticoagulation, those in whom D-dimer becomes positive will have their anticoagulation resumed and no longer discontinued. All patients will be followed up to completion of 4 years since recruitment. For the purpose of this study each quantitative D-dimer is allowed. The criterion for D-dimer interpretation will rely on the cut-off that is recommended by manufacturers for diagnostic purposes. D-dimer.For the purpose of this study each quantitative D-dimer is allowed. The criterion for D-dimer interpretation will rely on the cut-off that is recommended by manufacturers for diagnostic purposes. Sample size 1000 years of observation without anticoagulation are required to demonstrate (power 90%, type I error 0.05, two sided) that with this approach the annual rate of recurrent VTE is lower than 5%. Approximately 600 patients with proximal DVT satisfying the eligibility criteria are required to obtain 1000 years of observation without anticoagulation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis of Lower Limb, Lower Extremity Deep Venous Thrombosis Recurrent
Keywords
Deep venous thrombosis, Pulmonary embolism, Ultrasonography, D-dimer, Venous thromboembolism, Bleeding

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
584 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Proximal DVT
Arm Type
Experimental
Arm Description
Patients whose veins have recanalized (either at the recruitment or later on during the follow-up) will receive the D-dimer determination before discontinuing sodium warfarin. Veins are defined as recanalized when the vein diameter under maximum compressibility is lower than 4 mm both at the common femoral and at the popliteal vein. In those with negative D-dimer sodium warfarin will be discontinued. These patients will have two further determinations of D-dimer (after 1 and 3 months, respectively). While patients with persistently negative D-dimer will no longer receive sodium warfarin, those in whom D-dimer is positive or reverts to positive values in the following determinations will have their sodium warfarin resumed and no longer discontinued.
Intervention Type
Drug
Intervention Name(s)
Sodium warfarin
Other Intervention Name(s)
Vitamin K antagonists, Oral anticoagulants
Intervention Description
Patients with early vein recanalization, as shown by ultrasonography, and repeatedly negative D-dimer will have anticoagulation discontinued. They will be followed-up for up to 4 years after recruitment in order to assess the rate of recurrent symptomatic VTE. In all other patients anticoagulation will not be discontinued.
Primary Outcome Measure Information:
Title
Recurrent venous thromboembolism (VTE)
Description
To assess the rate of recurrent symptomatic VTE (expressed as rate/1000 patients-yeas) occurring after discontinuation of oral anticoagulant therapy up to the study conclusion.
Time Frame
Up to the study conclusion (see the study protocol)
Secondary Outcome Measure Information:
Title
Development of major bleeding complications
Description
To assess the rate of major or clinically relevant bleeding complications (expressed as rate/1000 patients-years) occurring during oral anticoagilant therapy up to the study conclusion
Time Frame
Up to the study conclusion (see the study protocol)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with proximal DVT that is idiopathic or secondary to minor factors for thrombosis, with or without contemporary manifestations of PE, who have completed an uneventful 3 to 24-month period of anticoagulation and are available for an overall 48-month follow-up at the study centre. Exclusion Criteria: previous thromboembolism recent (less than 3 months) major trauma or surgery active cancer immobilization resulting from chronic irreversible medical diseases need for indefinite anticoagulation for medical reasons other than VTE impossibility to attend the follow-up visits or to have D-dimer determinations already known major thrombophilia: carriage of deficiencies of natural anticoagulants, lupus-like anticoagulants, homozygosis for factor V Leiden or prothrombin mutation, heterozygosis for both abnormalities short (less than 1 year) life expectancy pregnancy age younger than 18 refusal of informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paolo Prandoni
Organizational Affiliation
Department of Cardiothoracic and Vascular Sciences, University of Padua
Official's Role
Principal Investigator
Facility Information:
Facility Name
Paolo Prandoni
City
Padua
ZIP/Postal Code
35028
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
28407492
Citation
Prandoni P, Vedovetto V, Ciammaichella M, Bucherini E, Corradini S, Enea I, Cosmi B, Mumoli N, Visona A, Barillari G, Bova C, Quintavalla R, Zanatta N, Pedrini S, Villalta S, Camporese G, Testa S, Parisi R, Becattini C, Cuppini S, Pengo V, Palareti G; Morgagni Investigators. Residual vein thrombosis and serial D-dimer for the long-term management of patients with deep venous thrombosis. Thromb Res. 2017 Jun;154:35-41. doi: 10.1016/j.thromres.2017.04.002. Epub 2017 Apr 4.
Results Reference
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Optimal Duration of Anticoagulation in Deep Venous Thrombosis

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