Study of Elastographic Properties of the Clot by Technical SWIRE (Shear Wave Induced Resonance Elastography) (ClotStruct)
Primary Purpose
Deep Vein Thrombosis
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
elastography SWIRE
Sponsored by
About this trial
This is an interventional treatment trial for Deep Vein Thrombosis focused on measuring blood coagulation, Endogenous Thrombin Potential, rotational thromboelastometry
Eligibility Criteria
Inclusion Criteria:
- Patient with proximal DVT, provoked or not, the symptomatology is less than 3d, with or without pulmonary embolism treated with heparin or oral anticoagulant
- Signed informed consent
- Patient affiliated to a social security scheme,
Exclusion Criteria:
- pregnant or lactating
- Life expectancy <1 month
- Patient with distal DVT or asymptomatic DVT accidental discovery
- Patient who underwent venous unclogging in acute phase
- exclusion period in another study,
- under administrative or judicial oversight, under guardianship
Sites / Locations
- University Hospital GrenobleRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Diagnosis of deep vein thrombosis
Arm Description
All subjects with proximal DVT will have quantitative elastography SWIRE, thrombin generation test and rotational thromboelastometry test.
Outcomes
Primary Outcome Measures
Change in in vivo elastographic properties of thrombus in patients with proximal deep vein thrombosis (DVT) through quantitative elastography
Secondary Outcome Measures
Thrombus properties depending on the existence or absence of pulmonary embolism (PE) associated
Thrombus properties if provoked versus unprovoked thrombosis
Correlation of the thrombus in vivo properties to the thrombin generation capacity and viscoelastic properties tested ex vivo by rotational thromboelastometry
Full Information
NCT ID
NCT02859532
First Posted
July 28, 2016
Last Updated
January 4, 2019
Sponsor
University Hospital, Grenoble
1. Study Identification
Unique Protocol Identification Number
NCT02859532
Brief Title
Study of Elastographic Properties of the Clot by Technical SWIRE (Shear Wave Induced Resonance Elastography)
Acronym
ClotStruct
Official Title
Study of Elastographic Properties of the Clot by Technical SWIRE (Shear Wave Induced Resonance Elastography)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (undefined)
Primary Completion Date
February 2019 (Anticipated)
Study Completion Date
February 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Deep vein thrombosis (DVT) is a vascular disease characterized by the formation of a thrombus within the venous system, mainly the lower limbs. The clot structure directly influences both its location, but also its progressive profile expansion material or regression and embolic migration.
Few data are available regarding the evolution of structural properties of thrombus after an acute episode of DVT. Thrombus formation is due to the polymerization of fibrinogen into fibrin. Fibrin is a viscoelastic polymer. Its mechanical properties directly determine how the thrombus responds to forces which it is subjected.
Determining the mechanical properties of the thrombus in vivo and ex vivo is expected to study its evolutionary properties.
Detailed Description
The main objective of the study is to characterize the in vivo properties of elastographic thrombus in patients with proximal deep vein thrombosis (DVT), for quantitative elastography performed at D0, D7, D30.
The ability to analyze the structural properties of the thrombus should allow us to then correlate these properties to the evolving nature of the thrombus (embolic migration or not, recanalization or not), and the effect of different treatment on the evolution of the thrombus
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis
Keywords
blood coagulation, Endogenous Thrombin Potential, rotational thromboelastometry
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Diagnosis of deep vein thrombosis
Arm Type
Experimental
Arm Description
All subjects with proximal DVT will have quantitative elastography SWIRE, thrombin generation test and rotational thromboelastometry test.
Intervention Type
Radiation
Intervention Name(s)
elastography SWIRE
Other Intervention Name(s)
Supersonic Imagine
Primary Outcome Measure Information:
Title
Change in in vivo elastographic properties of thrombus in patients with proximal deep vein thrombosis (DVT) through quantitative elastography
Time Frame
Day 0, Day 7, Day 30
Secondary Outcome Measure Information:
Title
Thrombus properties depending on the existence or absence of pulmonary embolism (PE) associated
Time Frame
Day 0, Day 7, Day 30
Title
Thrombus properties if provoked versus unprovoked thrombosis
Time Frame
Day 0, Day 7, Day 30
Title
Correlation of the thrombus in vivo properties to the thrombin generation capacity and viscoelastic properties tested ex vivo by rotational thromboelastometry
Time Frame
Day 0, Day 7, Day 30
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient with proximal DVT, provoked or not, the symptomatology is less than 3d, with or without pulmonary embolism treated with heparin or oral anticoagulant
Signed informed consent
Patient affiliated to a social security scheme,
Exclusion Criteria:
pregnant or lactating
Life expectancy <1 month
Patient with distal DVT or asymptomatic DVT accidental discovery
Patient who underwent venous unclogging in acute phase
exclusion period in another study,
under administrative or judicial oversight, under guardianship
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gilles PERNOD
Phone
00 334 767 657 17
Email
GPernod@chu-grenoble.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gilles PERNOD
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Grenoble
City
Grenoble
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gilles Pernod
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Study of Elastographic Properties of the Clot by Technical SWIRE (Shear Wave Induced Resonance Elastography)
We'll reach out to this number within 24 hrs