Contrast Enhanced Ultrasound and Muscle (Echomuscle)
Primary Purpose
Ischemia, Thromboangiitis Obliterans
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
contrast echographie with hexafluorur of sulfur
Sponsored by
About this trial
This is an interventional diagnostic trial for Ischemia
Eligibility Criteria
Inclusion Criteria:
- Men and women over 40 years
- Patients with chronic critical limb ischemia as defined by consensus TASC 2 and eligible to a revascularisation
- Objective evaluation of critical ischemia is based on ankle pressure < 70 mm Hg or toe pressure < 50 mm Hg for patients with ulcer or pressure ankle pressure < 50 mm Hg or toe pressure < 30 mm Hg for patients with rest pain.
- Patient's consent signed
Exclusion Criteria:
- Patients under 18
- Pregnant or breast feeding woman
- Burger's disease
Contra- indication to use of contrast
- Hypersensitivity to sulfurhexafluorure
- Unstable coronary heart disease, acute stroke, uncompensated heart failure
- Right to left shunt
- Serious pulmonary hypertension (> 90 mm Hg)
- Uncontroled increased blood pressure
- Acute respiratory distress syndrom
- Consent refused
- Patients with leg wounds preventing ultrasonography
Sites / Locations
- University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
revascularization group
Arm Description
Subjects in this arms have an contrast echographie with sonovue(r) then a revascularization and finnaly an other contrast echographie with sonovue.
Outcomes
Primary Outcome Measures
Time to Peak
Time to peak modification, before and one month after the revascularization
Secondary Outcome Measures
Curves datas
Evaluation of other data issued from the kinetic curve of enhancement (time between injection and peak, area under curve, quantitative value of peak, time of vein-muscle transit (TTP muscle -TTP vein) before and after revascularization.
kinetics values
Study of correlation between kinetic data (TTP) and measures of TcPO2 and toe systolic pressure before revascularization and one month after revascularization
Time to peak
Study of predictive value of TTP before revascularization on success of revascularization at 1 month (clinical evaluation on pain, lack of minor or major amputation, healing of ulcer) and at 3 months (survival, lack of minor or major amputation, new surgery).
Full Information
NCT ID
NCT02128750
First Posted
April 29, 2014
Last Updated
March 4, 2016
Sponsor
University Hospital, Grenoble
1. Study Identification
Unique Protocol Identification Number
NCT02128750
Brief Title
Contrast Enhanced Ultrasound and Muscle
Acronym
Echomuscle
Official Title
Echographie de Contraste Pour l'Analyse de la Perfusion Musculaire Dans l'ischémie Critique
Study Type
Interventional
2. Study Status
Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
March 2014 (Actual)
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
The primary objective of our work is to show that quantification of muscular microvascularisation evaluated by injection of contrast agent is different between chronic critical limb ischemia (before revascularization) and after (healing of ischemia) and thus make the proof of its utility in evaluation of PAD therapeutics.
Detailed Description
Peripheral arterial disease (PAD) is a frequent disease the incidence of which in men is about 32.5°/°° before 40 years and 71°/°° after 50 years. Prevalence of the disease increases with age to reach 3.7% of 60 to 69 year old subjects (Kannel 1970, 1985, Bloch 1985).
Critical limb ischemia (CLI) ischemia is defined by typical chronic ischemic rest pain or ischemic skin lesions either ulcers or gangrene for more than two weeks (Norgren). Incidence is about 500 - 1000 / 106 / year in Europe and United states. Critical limb ischemia concerns 15 - 20% of patients with intermittent claudication (Eneroth 1992, Taylor 1989). Development can lead to limb loss with a frequency estimated between 7% at 5 years to 12% at 10 years. Problem is crucial for patients who cannot benefit from revascularization. Results of single medical treatments are uncertain. Development of neovascularisation by innovating therapeutic (autolog cell stem grafts, intramuscular growth factor injections ) represent an exciting and promising field of research.
Peripheral arterial disease evaluation and staging are based on measures of resting ankle pressures, diagnosis of stenosis and obliteration (duplex, angiography, computed tomography scan and magnetic resonance imaging) and on measure of microcirculatory skin perfusion by Tc PO2. On the other hand, there is no simple tool to measure muscular microvascularisation whereas muscles suffer from ischemia in the same way as skin and nerves. Measures of muscular perfusion can be performed by Tc 99, magnetic resonance imaging but this is not used in clinical practice. CEUS used in routine to assess hepatic microvascularisation has recently been shown to be potentially useful to study muscle (Kramer 2008, Weber 2007).
Ultrasonic contrast agents are intravascular microbubbles which used at low mechanical index generate harmonics and allow real time imaging in ultrasonography. Their use allows study of parenchyma enhancement in real time, notably of liver and kidneys; they are also used in practice to differentiate benign and malign tumors (Correas 2009). Correlations have been shown between muscle enhancement studied by CEUS and histologic data of capillary vascularisation (Weber 2005). More recently some authors have shown that CEUS may allow to differentiate patients with PAD at a stage of intermittent claudication and patients without PAD (Duerschmied 2006).Very few studies have studied patients with CLI. Duerschmied and all have shown that kinetic data of muscle enhancement may reflect collateral circulation developed in reaction to chronic ischemia. CEUS may be used to study muscular perfusion in the same way as TcPO2 reflects cutaneous vascularisation and may become an evaluation criteria of PAD therapeutics in a near future.
We propose to study muscular perfusion by CEUS in patients with critical limb ischemia eligible to revascularization (PTA or bypass) before and after revascularization. Microbubbles injection leads to an increase in muscle echogenicity in two sequences: a rapid phase 15-20 s after injection (arteriolar filling) then a more intense second phase (veinular and capillary filling) (Duerschmied 2006). These two phases may be described by measures of acoustic intensity function of time and in particular time to peak (TTP), area under the curve (AUC). Time to peak seems to be the more reliable criteria (Duerschmied).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemia, Thromboangiitis Obliterans
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
32 (Actual)
8. Arms, Groups, and Interventions
Arm Title
revascularization group
Arm Type
Experimental
Arm Description
Subjects in this arms have an contrast echographie with sonovue(r) then a revascularization and finnaly an other contrast echographie with sonovue.
Intervention Type
Other
Intervention Name(s)
contrast echographie with hexafluorur of sulfur
Intervention Description
Echography of contrast after injection of product of contrast (sonovue (r))
Primary Outcome Measure Information:
Title
Time to Peak
Description
Time to peak modification, before and one month after the revascularization
Time Frame
M0 (before revascularisation) and M1 (One month after the revascularisation).
Secondary Outcome Measure Information:
Title
Curves datas
Description
Evaluation of other data issued from the kinetic curve of enhancement (time between injection and peak, area under curve, quantitative value of peak, time of vein-muscle transit (TTP muscle -TTP vein) before and after revascularization.
Time Frame
M0 (before revascularisation) M1 (one month after revascularisation).
Title
kinetics values
Description
Study of correlation between kinetic data (TTP) and measures of TcPO2 and toe systolic pressure before revascularization and one month after revascularization
Time Frame
M0 (before revascularisation) and M1 (one month after revascularisation).
Title
Time to peak
Description
Study of predictive value of TTP before revascularization on success of revascularization at 1 month (clinical evaluation on pain, lack of minor or major amputation, healing of ulcer) and at 3 months (survival, lack of minor or major amputation, new surgery).
Time Frame
M0, M1 and M3 (three month after revascularisation)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men and women over 40 years
Patients with chronic critical limb ischemia as defined by consensus TASC 2 and eligible to a revascularisation
Objective evaluation of critical ischemia is based on ankle pressure < 70 mm Hg or toe pressure < 50 mm Hg for patients with ulcer or pressure ankle pressure < 50 mm Hg or toe pressure < 30 mm Hg for patients with rest pain.
Patient's consent signed
Exclusion Criteria:
Patients under 18
Pregnant or breast feeding woman
Burger's disease
Contra- indication to use of contrast
Hypersensitivity to sulfurhexafluorure
Unstable coronary heart disease, acute stroke, uncompensated heart failure
Right to left shunt
Serious pulmonary hypertension (> 90 mm Hg)
Uncontroled increased blood pressure
Acute respiratory distress syndrom
Consent refused
Patients with leg wounds preventing ultrasonography
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christophe Seinturier, Doctor
Organizational Affiliation
University Hospital Grenoble - Medecine vasculaire
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital
City
Grenoble
ZIP/Postal Code
38000
Country
France
12. IPD Sharing Statement
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