ClinicalTrials.gg
CompletedNCT01756911STRATOUpdated Apr 14, 2014

Evaluation of the Safety and Efficacy of the Multilayer Stent

An interventional study of MFM in Aortic Aneurysm, Thoracoabdominal, Thoracoabdominal Aortic Aneurysm and Aortic Aneurysm, Thoracic, sponsored by Cardiatis. Completed at 9 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-04-14.

Sponsored by Cardiatis · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
23
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

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

Keywords

  • MFM
  • Multilayer Flow Modulator
  • Multilayer stent
  • Thoracoabdominal Aortic Aneurysm
03

In context

Aortic Aneurysm, Thoracoabdominal

63 studies on the registry are indexed under Aortic Aneurysm, Thoracoabdominal; 31 are open to participants now.

This study's enrollment of 23 is below the median of 80 across 41 interventional studies indexed under Aortic Aneurysm, Thoracoabdominal.

Browse Aortic Aneurysm, Thoracoabdominal studies →

Lead sponsor

Cardiatis is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age >18 years
  • ≥ 12 months
  • The patient or his legal representative has signed the 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)
  • 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 () 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. (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

Exclusion Criteria:

  • medical to a local or general anesthesia and angiography;
  • 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
Terms in these criteria, in plain language(5)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
23 participants (actual)

Study arms

  • Experimental
    Thotaco-abdominal aneurysm

    MFM

    Device: MFM

Interventions

  • DeviceMFM

    Implantation of the MFM

    Also known as: Multilayer Flow Modulator, Multilayer stent

06

What researchers measure

Primary outcomes

  1. Number of patients with aneurysm exclusion

    Time frame: 12 months

Secondary outcomes

  1. Number of covered branches permeable

    Time frame: 12 months

  2. Number of patients with Serious Adverse Events

    Time frame: 12 months

07

Study locations

9 sites
  • Hopital Jean Minjoz
    Besançon, 25030, France
  • Hopital Neurocardiologique
    Bron, 69677, France
  • Centre Hospitalier de La Région D'Annecy
    Metz-Tessy, 74370, France
  • Chu Brabois Nancy
    Nancy, 54511, France
  • Hopital Europeen Georges-Pompidou
    Paris, 75015, France
  • Pitie-Salpetriere
    Paris, 75651, France
  • CMC Parly II
    Paris, 78150, France
  • Institut Cardio-Vasculaire Paris Sud Hôpital Claude Galien À Quincy
    Quincy-sous-Sénart, 91480, France
  • Hopital Universitaire Rangueil
    Toulouse, 31059, France
08

References and documents

Publications

  • 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. PubMed 24502488 ↗
  • 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. PubMed 27280802 ↗
09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Mar 2010, a primary completion of Apr 2012 and a completion of Apr 2012. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 14, 2012
First posted
Dec 28, 2012
Start
Mar 2010
Primary completionActual
Apr 2012
CompletionActual
Apr 2012
Last update
Apr 14, 2014
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 14, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01756911
Lead sponsor
Cardiatis
Responsible party
Sponsor
First posted
Dec 28, 2012
Start date
Mar 2010
Primary completion
Apr 2012
Completion
Apr 2012
Last update
Apr 14, 2014

Study contacts

Jean-Noël Fabiani, Pr
principal investigator · HEGP

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2014. You cannot join it, but the record below documents what was studied.

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