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Aortic Aneurysm, ThoracoabdominalSTRATONCT01756911

Evaluation of the Safety and Efficacy of the Multilayer Stent

A study testing MFM in people with Aortic Aneurysm, Thoracoabdominal and Thoracoabdominal Aortic Aneurysm, run by Cardiatis at 9 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
MFM
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
23 participants
Where
9 sitesFrance
Study dates
Mar 2010to Apr 2012
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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
Show all 21Show fewer
  • 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.

Who cannot join

  • 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

Trial locations and contacts

9 sites in 1 country.

9 sites in 1 country

France9 sites
  • Hopital Jean Minjoz

    Besançon, 25030

  • Hopital Neurocardiologique

    Bron, 69677

  • Centre Hospitalier de La Région D'Annecy

    Metz-Tessy, 74370

  • Chu Brabois Nancy

    Nancy, 54511

  • Hopital Europeen Georges-Pompidou

    Paris, 75015

  • Pitie-Salpetriere

    Paris, 75651

  • CMC Parly II

    Paris, 78150

  • Institut Cardio-Vasculaire Paris Sud Hôpital Claude Galien À Quincy

    Quincy-sous-Sénart, 91480

  • Hopital Universitaire Rangueil

    Toulouse, 31059

Other trials in France

About this study

Official title: Evaluation du Stent Multicouches Dans le Traitement Des anévrismes de l'Aorte Thoraco-abdominale

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.

Being tested
MFM
Keywords
MFM, Multilayer Flow Modulator, Multilayer stent, Thoracoabdominal Aortic Aneurysm
Medical subject headings
Aortic Aneurysm, Thoracoabdominal, Aortic Aneurysm, Thoracic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MFMDevice

    Also called Multilayer Flow Modulator, Multilayer stent

    Implantation of the MFM

Study groups in NCT01756911
Study groupRoleWhat they receive
Thotaco-abdominal aneurysmExperimentalMFM
Receives: Device: MFM

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of patients with aneurysm exclusion

    Measured: 12 months

Secondary outcomes (2)
  1. Number of covered branches permeable

    Measured: 12 months

  2. Number of patients with Serious Adverse Events

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Dec 2012 (estimated)
  2. Study startMar 2010
  3. Primary completionApr 2012
  4. Study completionApr 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
23 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01756911
Sponsor's protocol ID
IC_0308_FRA
Other IDs
2009-013678-42, 2009
Acronym
STRATO
Status last verified
Apr 2014
First submitted
14 Dec 2012
Last updated
14 Apr 2014
Results posted
No
Data monitoring committee
Yes

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

Questions about this trial

What is this clinical trial studying?

A study testing MFM in people with Aortic Aneurysm, Thoracoabdominal and Thoracoabdominal Aortic Aneurysm, run by Cardiatis at 9 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 21 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Apr 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 9 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of patients with aneurysm exclusion (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01756911, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Apr 2014.

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