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Evaluation of the Safety and Efficacy of the Multilayer Stent (STRATO)

Primary Purpose

Aortic Aneurysm, Thoracoabdominal, Thoracoabdominal Aortic Aneurysm, Aortic Aneurysm, Thoracic

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
MFM
Sponsored by
Cardiatis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aortic Aneurysm, Thoracoabdominal focused on measuring MFM, Multilayer Flow Modulator, Multilayer stent, Thoracoabdominal Aortic Aneurysm

Eligibility Criteria

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

Inclusion Criteria:

  • Age >18 years
  • Life expectancy ≥ 12 months
  • The patient or his legal representative has signed the informed consent form
  • Thoracoabdominal aneurysm type 2 or 3 with vital collaterals and requiring intervention to prevent its rupture according to the criteria defined by consensus ("Expert Consensus Document on the Treatment of Descending Thoracic Aortic Disease Using Endovascular Stent-Grafts", Ann Thorac Surg 2008;85:S1-41)
  • Contraindicated for open surgery, declared inoperable by the surgeon and anesthetist (statement signed by each doctor) and must have at least one of the following:

    1. Age > 80 years
    2. ASA (American Society of Anesthesiologists) score ≥ 3
    3. History of thoracic surgery or surgery of the abdominal aorta
    4. Coronary artery disease (history of angina or myocardial infarction) with positive functional testing and coronary lesions for which revascularization is impossible or not indicated
    5. Heart failure
    6. Inoperable aortic stenosis
    7. LVEF (Left Ventricular Ejection Fraction) <40%;
    8. chronic respiratory failure defined by one of the following criteria:

      1. FEV (Forced expiratory volume) <1.2 l / sec;
      2. VC (Vital Capacity) <50% of the predicted value according to age, sex and weight;
      3. arterial blood gas analysis in the absence of oxygen: PaCO2 (Pression artérielle en CO2) > 45 mmHg or PaO2 (Pression artérielle en O2) <60 mmHg
      4. Oxygen therapy
    9. renal insufficiency if creatininaemia> 200 micromol / l before injection of contrast product;
    10. hostile abdomen, including presence of ascites or other signs of portal hypertension;
    11. obesity.
  • adequate arterial anatomy of aneurismal lesion access.

Exclusion Criteria:

  • medical contraindications to a local or general anesthesia and angiography;
  • Life expectancy less than one year, or clinical follow-up impossible;
  • congenital disorders of blood coagulation;
  • intercurrent infection;
  • allergy to aspirin, clopidogrel, or contrast agents;
  • patient(s) included in another clinical study;
  • patient pregnant or breastfeeding

Sites / Locations

  • Hopital Jean Minjoz
  • Hopital Neurocardiologique
  • Centre Hospitalier de La Région D'Annecy
  • Chu Brabois Nancy
  • Hopital Europeen Georges-Pompidou
  • Pitie-Salpetriere
  • CMC Parly II
  • Institut Cardio-Vasculaire Paris Sud Hôpital Claude Galien À Quincy
  • Hopital Universitaire Rangueil

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Thotaco-abdominal aneurysm

Arm Description

MFM

Outcomes

Primary Outcome Measures

Number of patients with aneurysm exclusion

Secondary Outcome Measures

Number of covered branches permeable
Number of patients with Serious Adverse Events

Full Information

First Posted
December 14, 2012
Last Updated
April 11, 2014
Sponsor
Cardiatis
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1. Study Identification

Unique Protocol Identification Number
NCT01756911
Brief Title
Evaluation of the Safety and Efficacy of the Multilayer Stent
Acronym
STRATO
Official Title
Evaluation du Stent Multicouches Dans le Traitement Des anévrismes de l'Aorte Thoraco-abdominale
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
March 2010 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cardiatis

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Evaluation of the Multilayer Flow Modulator (MFM) for Endovascular Thoracoabdominal Aneurysm Repair. The objectives of the study is to determine the efficacy, safety and performance of the MFM and its delivery system in patients at high surgical risk presenting with a type II, III thoracoabdominal aneurysm, below the left subclavian and above the iliac bifurcation, according to the Crawford classification.
Detailed Description
Conventional treatments of thoracoabdominal aneurysm are medical treatments (based on hypertension control) on one hand and surgical treatment on the other hand. The standard treatment is surgery consisting of an exclusion of the aneurysm with restoration of continuity by means of a prosthesis usually made of Dacron. The rates of surgical morbidity and mortality differ according to whether the patient is treated electively or in an emergency setting. The most feared complication is spinal cord ischemia inducing paraplegia. In elective surgery, operative mortality is estimated to be between 6% and 15% depending on the series, and around 50% to 60% of patients are treated in an emergency setting. The rate of neurological complications such as paraparesis or paraplegia is estimated to be between 3% and 15%. In addition to the above, the following major complications have been shown to have an impact on the morbidity of this major surgery (5% each): Bleeding requiring surgical hemostasis Respiratory distress syndrome requiring prolonged ventilation support Acute renal failure Infections Central neurological events (stroke and coma) Peripheral neurological events (sensory-motor deficits, paraparesis, paraplegia) Analyses identify risk factors increasing the morbidity and mortality: Patients over 80 years Chronic obstructive pulmonary disease Renal failure Coronary artery disease Comorbidities (malignancy, etc.) Compared to surgery, endovascular stenting reduces: Pulmonary morbidity (suppression of thoracotomy and ventilation), in patients with impaired lung function; Renal dysfunction; Myocardial failure; Risk of spinal cord ischemia and paraplegia. However, this treatment has a number of limitations Availability of device in case of emergency Topography of the neck must be far enough from the left subclavian artery to allow satisfactory fixation of the stent and exclusion of the lesion; Obstruction of the branches near the aneurysm. In the current available treatment for this pathology, there are still some disadvantages such as the difficulty of precise positioning of the prosthesis and its branches which must cover the aneurysm tissue without endoleaks. Each lesion having anatomical specificities, the device must be designed for each individual patient, and the operator's technical ability must be extreme. So, the current technique is difficult to reproduce, and any emergency treatment is impossible. The multilayer flow modulator (non-covered) is the device used in this trial The complications mentioned above are inherent in the concept of covered stent treatment plus endoleaks that continues to fuel the aneurismal sac untreated, thus subject to the persistent risk of rupture. With this technique, the visceral arteries are occluded or have a retrograde flow (which pressurizes the aneurysm again). The multilayer flow modulator (non-covered) treatment approach avoids the major problems mentioned above: It allows the aneurismal sac to thrombose whilst maintaining the patency of collateral branches arising from the aneurysm; It improves the flow in the collateral branches, which becomes laminar flow through a mechanism of hemodynamic pressure drop from layer to layer and an increase in speed by rolling; Deployment is easier and it is not different from peripheral stent deployment; The device is available in all sizes and all lengths that can be stored, allowing the management of emergencies. The space-age 3D geometrical design of a Cardiatis multilayer flow modulator modifies flow within the aorta in a way that reduces pressure within the aneurysm thus collapsing the aneurismal sac while preserving any vital collateral circulation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Aneurysm, Thoracoabdominal, Thoracoabdominal Aortic Aneurysm, Aortic Aneurysm, Thoracic
Keywords
MFM, Multilayer Flow Modulator, Multilayer stent, Thoracoabdominal Aortic Aneurysm

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
23 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Thotaco-abdominal aneurysm
Arm Type
Experimental
Arm Description
MFM
Intervention Type
Device
Intervention Name(s)
MFM
Other Intervention Name(s)
Multilayer Flow Modulator, Multilayer stent
Intervention Description
Implantation of the MFM
Primary Outcome Measure Information:
Title
Number of patients with aneurysm exclusion
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of covered branches permeable
Time Frame
12 months
Title
Number of patients with Serious Adverse Events
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >18 years Life expectancy ≥ 12 months The patient or his legal representative has signed the informed consent form Thoracoabdominal aneurysm type 2 or 3 with vital collaterals and requiring intervention to prevent its rupture according to the criteria defined by consensus ("Expert Consensus Document on the Treatment of Descending Thoracic Aortic Disease Using Endovascular Stent-Grafts", Ann Thorac Surg 2008;85:S1-41) Contraindicated for open surgery, declared inoperable by the surgeon and anesthetist (statement signed by each doctor) and must have at least one of the following: Age > 80 years ASA (American Society of Anesthesiologists) score ≥ 3 History of thoracic surgery or surgery of the abdominal aorta Coronary artery disease (history of angina or myocardial infarction) with positive functional testing and coronary lesions for which revascularization is impossible or not indicated Heart failure Inoperable aortic stenosis LVEF (Left Ventricular Ejection Fraction) <40%; chronic respiratory failure defined by one of the following criteria: FEV (Forced expiratory volume) <1.2 l / sec; VC (Vital Capacity) <50% of the predicted value according to age, sex and weight; arterial blood gas analysis in the absence of oxygen: PaCO2 (Pression artérielle en CO2) > 45 mmHg or PaO2 (Pression artérielle en O2) <60 mmHg Oxygen therapy renal insufficiency if creatininaemia> 200 micromol / l before injection of contrast product; hostile abdomen, including presence of ascites or other signs of portal hypertension; obesity. adequate arterial anatomy of aneurismal lesion access. Exclusion Criteria: medical contraindications to a local or general anesthesia and angiography; Life expectancy less than one year, or clinical follow-up impossible; congenital disorders of blood coagulation; intercurrent infection; allergy to aspirin, clopidogrel, or contrast agents; patient(s) included in another clinical study; patient pregnant or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Noël Fabiani, Pr
Organizational Affiliation
HEGP
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital Jean Minjoz
City
Besançon
ZIP/Postal Code
25030
Country
France
Facility Name
Hopital Neurocardiologique
City
Bron
ZIP/Postal Code
69677
Country
France
Facility Name
Centre Hospitalier de La Région D'Annecy
City
Metz-Tessy
ZIP/Postal Code
74370
Country
France
Facility Name
Chu Brabois Nancy
City
Nancy
ZIP/Postal Code
54511
Country
France
Facility Name
Hopital Europeen Georges-Pompidou
City
Paris
ZIP/Postal Code
75015
Country
France
Facility Name
Pitie-Salpetriere
City
Paris
ZIP/Postal Code
75651
Country
France
Facility Name
CMC Parly II
City
Paris
ZIP/Postal Code
78150
Country
France
Facility Name
Institut Cardio-Vasculaire Paris Sud Hôpital Claude Galien À Quincy
City
Quincy-sous-Sénart
ZIP/Postal Code
91480
Country
France
Facility Name
Hopital Universitaire Rangueil
City
Toulouse
ZIP/Postal Code
31059
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
24502488
Citation
Vaislic CD, Fabiani JN, Chocron S, Robin J, Costache VS, Villemot JP, Alsac JM, Leprince PN, Unterseeh T, Portocarrero E, Glock Y, Rousseau H; STRATO Investigators Group. One-year outcomes following repair of thoracoabdominal aneurysms with the multilayer flow modulator: report from the STRATO trial. J Endovasc Ther. 2014 Feb;21(1):85-95. doi: 10.1583/13-4553R.1.
Results Reference
result
PubMed Identifier
27280802
Citation
Vaislic CD, Fabiani JN, Chocron S, Robin J, Costache VS, Villemot JP, Alsac JM, Leprince PN, Unterseeh T, Portocarrero E, Glock Y, Rousseau H; STRATO Investigators Group. Three-Year Outcomes With the Multilayer Flow Modulator for Repair of Thoracoabdominal Aneurysms: A Follow-up Report From the STRATO Trial. J Endovasc Ther. 2016 Oct;23(5):762-72. doi: 10.1177/1526602816653095. Epub 2016 Jun 8.
Results Reference
derived
Links:
URL
http://www.ncbi.nlm.nih.gov/pubmed/24502488
Description
One-year outcomes following repair of thoracoabdominal aneurysms with the multilayer flow modulator: report from the STRATO trial

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Evaluation of the Safety and Efficacy of the Multilayer Stent

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