SPIRIT: Study of the Patency of Spinal aRteries After the STABILISE Technique
NCT ID: NCT06373393
Last Updated: 2024-04-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
50 participants
OBSERVATIONAL
2024-04-16
2024-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Primary end-point: patency of the intercostal and lumbar arteries on follow-up CTA.
Secondary end-point: spinal cord ischaemia
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Registry of Patients With Acute/Subacute Type B Aortic Dissection Treated by Means of the STABILISE Technique (STABILISE)
NCT03707743
Predilation of Side Branch During Percutaneous Treatment of Bifurcation Lesions With Provisional T Stenting
NCT01090856
Use of Interlocking Detachable Coils System in Embolization of Peripheral Arterial Embolization
NCT05391399
Jailed Wire Technique in the Treatment of Coronary Bifurcations Lesions With Stent: Stereoscopic Microscopy Study
NCT02516891
Efficacy and Safety of Sirolimus-Coated Spiral Balloon for Coronary Bifurcation Lesions
NCT06618248
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Endovascular treatment emerged over the last decade as the standard of care for complicated acute type B aortic dissection and the first step is usually the deployment of a thoracic endograft (TEVAR) aiming to cover the entry tear. TEVAR may be enough to fix malperfusion syndromes but is frequently associated with late aortic dilatation and unfavorable remodeling \[1,2\]. The failure of simple TEVAR to solve malperfusion syndromes led to the development of adjunctive techniques like direct stenting of the occluded arteries, fenestration of the lamella or the association of a self-expandable bare stent deployment across the visceral and renal arteries to increase the true lumen diameter and improve perfusion of those arteries.
The STABILISE technique to treat type B dissections is able to disrupt the lamella of the dissected aorta and consequently restore the uniluminal state of the aortic anatomy \[3,4,5\].
The dissection process is related to the detachment of the aortic side branch ostia (visceral, renal, iliacs, intercostals, lumbars) and therefore a potential status of malperfusion which is often related to severe clinical complications that should be properly managed. Additionally, when the lamella is brought back to the peripheral aortic wall, according to the STABILISE concept, the recovery of perfusion from the true lumen is unclear.
All these mechanisms, as well as the cover of the ostia of upper intercostal arteries by the stentgraft, may compromise the intercostal and lumbar arteries patency or the direct flow from the true lumen and therefore be related to the occurrence of spinal cord ischemia complications which prevalence was not yet determined \[6-10\].
FEASIBILITY AND PRELIMINARY DATA
Our research group carried out a pilot study, accepted for publication in the journal "Journal of Vascular Surgery Cases, Innovations and Techniques", on patency of intercostal arteries after treatment of type B aortic dissection with the STABILIZE technique. In this study, we observed a decrease in the permeability of the intercostal arteries in the area of the thoracic endoprosthesis, but we concluded that the permeability of the spinal arteries was not significantly affected by the coverage of the aorta with the uncovered stent nor by its aggressive ballooning to replace the intimal lamella. These findings constitute a step towards a better understanding of the safety of this technique.
STUDY DESIGN AND METHODS
This is a multi-center, non-randomized, retrospective observational analysis of patients treated with STABILISE technique for type B aortic dissection.
The following data will be collected:
* preoperative comorbidities.
* temporal phase of dissection (hyperacute, acute, subacute or chronic).
* procedural data (diameter and length of the stentgraft(s) and bare stent(s) and length of the covered aorta.
* occurrence of SCI at discharge and 30 days after procedure, according to the TARLOV scale.
Contrast-enhanced thoraco-abdominal CTA will be performed to patients pre-operatively and within 1 month, 6 months and yearly after the procedure.
Inclusion criteria
All patients with ≥ 18 years of age, with a type B dissection, treated according to the STABILISE technique
Exclusion criteria
\- Aortic rupture.
CTA protocol Contrast-enhanced thoraco-abdominal CTA (with thin slices, preferably 1mm) will be performed to all patients pre-operatively and within 1 month, 6 months and then yearly after the procedure. Axial, coronal and column curvature based maximum intensity projections (MIP) with 10mm slice thickness will be performed and analyzed retrospectively.
After removing any patient's identification, the DICOM data will be sent, via WeTransfer, to the analysis center in Lisbon where the quantification and patency analysis will be performed.
Results evaluation The CTA images will be semi-quantitatively analyzed by two independent investigators and the number of visible intercostal and lumbar arteries in the stented aorta (stent-graft and dilated bare metal stent) will be evaluated.
The following parameters will be analyzed and reported in the attached sheet:
PRE-TREATMENT CTA
* Presence and patency of the intercostal and lumbar arteries specifying right and left sides.
* Origin of the intercostal and lumbar arteries - true lumen, false lumen (FL), both - specifying right and left sides
POST-TREATMENT CTA's
* Presence and patency of the intercostal and lumbar arteries (specifying right and left sides).
* Origin of the intercostal and lumbar arteries (TL, FL, both) in cases where the uniluminal state was not completely restored (specifying right and left sides).
* Patency of the distal portion of the intercostal and lumbar arteries when the ostium was covered by the stentgraft (specifying right and left sides).
* Patency of the intercostal and lumbar arteries in the area of the bare stent (specifying right and left sides).
* Patency of the intercostal and lumbar arteries in the area distal to the bare stent (specifying right and left sides).
All the assessed variables will be collected at the coordinating Center (Santa Maria Hospital), using the image data provided by the two participating centers.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
STABILISE
STABILISE technique: "Stent assisted balloon induced intimal disruption and relamination in aortic dissection repair"
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
100 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cardiovascular Center of the University of Lisbon
UNKNOWN
Unidade Local de Saúde Santa Maria
OTHER_GOV
Associacao para Investigacao e Desenvolvimento da Faculdade de Medicina - CETERA
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Unidade Local de Saúde Santa Maria
Lisbon, , Portugal
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.