Thoracic Aortic Dissection

5

Review clinical trials related to Thoracic Aortic Dissection. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

MBA Early Feasibility Study

The MBA 25-04 study is a prospective, multicenter, non-randomized, single-arm, early feasibility study designed to assess the initial safety of the MBA device through five years following the index endovascular procedure.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: W.L.Gore & AssociatesUpdated: Jun 1, 2026
Eligibility criteria

Anatomic compatibility with MBA device and other devices required for proximal o... [+19]

De novo Type A dissection [+29]

Status: Recruiting

Antibacterial Tactics Based on Presepsin Level in Thoracic Aorta Surgery Patients

According to the literature, presepsin was recommended not only as an effective indicator in the diagnosis of sepsis in intensive care units, but also as a reliable prognostic marker of postoperative inflammatory processes in cardiac surgery. Previous study carried out in Petrovsky NRCS related to biomarkers in cardiac surgery and presepsin in particular showed good sensitivity in infection complications prognosis.

Participants needed: 50
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Petrovsky National Research Centre of SurgeryUpdated: Jan 29, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Impact of Right Atrial Occlusion on TEVAR Outcomes

Though the application of thoracic endovascular aortic repair (TEVAR) for treatment of aortic pathology is expanding, there remains a gap in the literature examining how intraoperative "reduction or elimination of aortic impulse" (REAI) techniques, in particular the use of right atrial occlusion, may impact patient important clinical outcomes. This study aims to provide prospective data from a large cohort of TEVAR patients to explore clinical outcomes following TEVAR procedures and, specifically, whether right atrial occlusion has significant impact on clinical outcomes, as compared to other REAI techniques. The results from this study may inform future perioperative TEVAR practices and improve TEVAR patient outcomes.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of CalgaryUpdated: Jun 29, 2025
Eligibility criteria

age 18 years or older [+3]

age 18 years or younger [+3]

Status: Recruiting

Post-market Clinical Trial of the Dominus® Stent-Graft

Real-world clinical trial evidence post-market, evaluating the safety and efficacy of the Dominus® StentGraft Endoprosthesis in treating thoracic aortic diseases, following the Instructions for Use

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Braile Biomedica Ind. Com. e Repr. Ltda.Updated: Aug 22, 2024Locations: 3
Eligibility criteria

18 years of age or older; [+3]

Patient currently participating in another clinical study of drug or medical dev... [+1]

Status: Recruiting

ENDOBARC-S Study: "Endovascular Branched Stent-grafts for Aortic ARCh Pathologies in Spain"

The ENDOBARC-S post-market clinical follow-up study is undertaken to evaluate the prevention of death related to aortic arch pathologies when treated by branch stent graft systems (Nexus stent-graft system®, Relay Branch® or Zenith arch branch graft®), with proximal landing at zone 0. The secondary objective is to evaluate the safety and clinical performance of the studied devices.

Participants needed: 100
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Vascular Investigation Network Spanish Society for Angiology and Vascular SurgeryUpdated: Apr 4, 2022Locations: 1Duration: 5 Years
Eligibility criteria

Patient is between 18 and 90 years old [+3]

Patient less than 18 years old or more than 90 years old. [+8]