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Paraplegia Prevention in Aortic Aneurysm Repair by Thoracoabdominal Staging

Paraplegia Prevention in Aortic Aneurysm Repair by Thoracoabdominal Staging With 'Minimally-Invasive Segmental Artery Coil-Embolization': A Randomized Controlled Multicentre Trial - PAPAartis

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03434314
Acronym
PAPAartis
Enrollment
500
Registered
2018-02-15
Start date
2018-11-08
Completion date
2025-06-30
Last updated
2024-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Aneurysm, Thoracoabdominal

Keywords

Paraplegia, Aortic Aneurysm Repair, Staging, Embolization, TAAA, Thoracoabdominal aortic aneurysm, MISACE, Spinal cord ischemia, Spinal cord ischaemia, Spinal cord injury, Spinal cord ischemic injury, Spinal cord ischaemic injury, Permanent paraplegia, Temporary paraplegia, Paraparesis, SCI, TAAA repair, Open TAAA repair, Open surgical TAAA repair, Endovascular TAAA repair, TEVAR, Aortic surgery, Thoracoabdominal aortic surgery, Type B aortic dissection, Chronic type B aortic dissection, Stanford type B aortic dissection, Collateral network, Paraspinal collateral network, Paraspinous collateral network, Arteriogenesis, Intercostal arteries

Brief summary

Aortic aneurysms represent the most common and dangerous aortic diseases. Although conventional aortic repair techniques cure the disease, there is a high risk of paraplegia particularly in extensive thoracoabdominal aneurysms due to impaired blood supply to the spinal cord. The PAPA-ARTiS trial will assess the clinical safety and efficacy of the MISACE (Minimally-Invasive Segmental Artery Coil-Embolization) procedure, a novel therapeutic concept to reduce the risk of paraplegia due to aneurysm repair. The study investigates the MISACE procedure as a potential pre-treatment prior to open or endovascular aneurysm repair in patients with thoracoabdominal aortic aneurysms. Patients will be randomized to one of the two treatment strategies: a) aneurysm repair without MISACE pre-treatment, or b) aneurysm repair with MISACE pre-treatment.

Detailed description

Chronic aortic aneurysms are permanent and localized dilations of the aorta that remain asymptomatic for long periods of time, but continue to increase in diameter before they eventually rupture. Left untreated, the patients' prognosis is dismal, since the internal bleeding of the rupture brings about sudden death. Although successful treatment cures the disease, the risky procedures compromise spinal cord blood supply acutely and permanently, frequently leading to paraplegia, particularly for aneurysms involving crucial segmental arteries, i.e. thoracoabdominal aortic aneurysms of Crawford type II & III. Although various strategies have achieved a remarkable decrease in the incidence of paraplegia, it is still no less than 10-20%. However, it has recently been found that the deliberate staged occlusion of the segmental arteries to the paraspinous collateral network finally supplying the spinal cord can trigger arterial collateralization, thus stabilizing blood supply from alternate inflow sources and preventing ischaemia. This has been translated to a clinically available therapeutic option, 'minimally invasive staged segmental artery coil embolization' (MISACE), which proceeds in a 'staged' manner to occlude groups of arteries under highly controlled conditions, after which time must be allowed for arteriogenesis to build a robust collateral blood supply. PAPA-ARTiS is a multi-national, prospective, open-label, two-arm, randomized controlled trial to demonstrate, that a minimally invasive staged treatment approach can reduce paraplegia and mortality in patients undergoing thoracoabdominal aortic aneurysm (TAAA) repair. Patients with planned aneurysm repair will be included in the study and will be randomized 1:1 in the control group or the MISACE-group. The control group receives treatment as per standard institutional protocol - open or endovascular repair without MISACE. In the MISACE-group, segmental arteries will be occluded in one to three sessions some weeks before the definite repair. Segmental arteries are occluded with coils or plugs.This induces arteriogenesis and the building of a robust collateral network ultimately supplying the spinal cord. During aneurysm repair, these new arteries provide an alternate blood supply to the spinal cord and thereby help prevent paraplegia.

Interventions

PROCEDUREMinimally-Invasive Segmental Artery Coil-Embolization

During one single MISACE session 3-7 segmental arteries will be occluded. The procedure is conducted through a peripheral artery access in local anaesthesia. Microcoils or vascular plugs will be used for the occlusion itself.

Sponsors

European Commission
CollaboratorOTHER
German Research Foundation
CollaboratorOTHER
Universidad de Granada
CollaboratorOTHER
European Clinical Research Infrastructure Network
CollaboratorOTHER
Modus Research and Innovation Limited
CollaboratorUNKNOWN
Rigshospitalet, Denmark
CollaboratorOTHER
European Society of Cardiology
CollaboratorNETWORK
Baylor College of Medicine
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
University of Leipzig
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* TAAA, Crawford type II or III * planned open or endovascular repair of aneurysm within four months * ≥ 18 years old

Exclusion criteria

* complicated (sub-) acute type B aortic dissection * ruptured and urgent aneurysm (emergencies) * untreated aortic arch aneurysm * bilaterally occluded iliac arteries or chronic total occlusion of left subclavian artery * pre-operative neurological deficits or spinal cord dysfunction * major untreated cardio-pulmonary disease * life-expectancy of less than one year * high risk for segmental artery embolism * severe contrast agent allergy, severe reduction in glomerular filtration rate (CKD stage 4) * expected lack of compliance * pregnant or nursing women * impaired thyroid function, if not under stable treatment * women of child bearing potential without highly effective contraceptive measures * current participation in other interventional clinical trial * patients under legal supervision or guardianship * patients placed in an institution by official or court order

Design outcomes

Primary

MeasureTime frameDescription
The primary objective is to greatly reduce incidence of ischaemic spinal cord injury and mortality.30 days after TAAA repairSuccessful treatment of the aneurysm is a binary variable. All of the following criteria must be met for this composite endpoint to count as a success: * The patient is alive and without substantial spinal cord injury 30 days after treatment, and * the aneurysm did not rupture and has been excluded within six months of randomization. Substantial spinal cord injury will be determined with a modified Tarlov scale (see below).

Secondary

MeasureTime frameDescription
spinal cord injury according to the modified Tarlov scale from TAAA repair to one yearfrom date of TAAA repair and up to one year after TAAA repairSpinal cord injury will be determined with a modified Tarlov scale (see above).
mortalityat 30 days and one year after TAAA repairall-cause mortality
stay in intensive care unit and intermediate carefrom date of TAAA repair and up to one year after TAAA repairlength of stay in intensive care unit and intermediate care unit after TAAA repair
sub-group analysesup to one year after TAAA repairsub-group analyses of spinal cord injury according to modified Tarlov scale (see above) for open repair and endovascular repair separately
substantial spinal cord injury30 days after TAAA repair and at one year after TAAA repairSubstantial spinal cord injury is defined as zero to two on the modified Tarlov scale. 0\. No lower extremity movement 1. Lower extremity motion without gravity 2. Lower extremity motion against gravity 3. Able to stand with assistance 4. Able to walk with assistance 5. Normal
cross-clamping timesduring open surgerycross-clamping times during open surgery
residual aneurysm sac perfusionup to one year after TAAA repairresidual aneurysm sac perfusion, i.e. type II endoleaks (only for endovascular repair)
costsup to one year after TAAA repairincremental cost-effectiveness ratio (ICER) will be calculated
Quality Adjusted Life Yearsup to one year after TAAA repairQuality Adjusted Life Years (QALYs) will be estimated over one year
re-operation for bleedingfrom date of TAAA repair and up to one year after TAAA repairre-operation for bleeding (only for open repair)

Countries

Austria, France, Germany, Italy, Netherlands, Poland, Sweden, Switzerland, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026