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Aortic Dissection clinical trials

View clinical trials related to Aortic Dissection.

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NCT ID: NCT06289777 Not yet recruiting - Clinical trials for Type B Aortic Dissection

Aortic Remodeling After Endovascular Management of Type B Aortic Dissection.

Start date: March 1, 2024
Phase:
Study type: Observational

Assess the clinical outcome, morphological changes and behaviour of type B aortic dissection after endovascular repair.

NCT ID: NCT06276413 Not yet recruiting - Aortic Dissection Clinical Trials

REgistRy BRAnch goRE EndopRosthEsis

REBRA
Start date: March 1, 2024
Phase:
Study type: Observational [Patient Registry]

Multicenter registry on patients treated by the new Gore thoracic branched endoprosthesis

NCT ID: NCT06270537 Recruiting - Clinical trials for Thoracic Aortic Dissection

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

DominusPMCF
Start date: October 24, 2023
Phase:
Study type: Observational

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

NCT ID: NCT06261411 Enrolling by invitation - Thoracic Surgery Clinical Trials

Lung Ultrasound as Alternative to Radiation in Thoracic Surgery

LUS-ART
Start date: February 12, 2024
Phase: N/A
Study type: Interventional

This projects aim is to study the effects of substitute conventional chest x-ray with lung ultrasound for patients undergoing thoracic surgery. Participants in the study will be randomized to either ultrasound or routine chest x-ray as the primary method of diagnosis after having received surgery to their lungs.

NCT ID: NCT06256757 Not yet recruiting - Clinical trials for Aortic Dissection Aneurysm

Safety and Validity of Extracorporeal Fenestration and in Situ Fenestration in Patients With Aortic Disease Involving the Left Subclavian Artery

Start date: May 1, 2024
Phase: N/A
Study type: Interventional

This trial aims to demonstrate the safety and validity of extracorporeal fenestration and in situ fenestration in patients with aortic disease involving the left subclavian artery.

NCT ID: NCT06235619 Not yet recruiting - Aneurysm Clinical Trials

Arch Size Study for Anatomical Variations

Start date: September 2024
Phase:
Study type: Observational

The aortic arch with a common origin of the innominate and left carotid artery (CILCA) prevalence in the general population is 13.6%. Its reputation as a benign anatomical variant has been ultimately shattered by further studies [3, 4, 8, 9] that identified the CILCA arch as a potential marker for thoracic aortic disease (TAD) The aim of this work is to report the CT anatomical characteristics of the aortic arch in subjects with or without aneurysms requiring treatment, in 5 major European cardiovascular centers.

NCT ID: NCT06199401 Not yet recruiting - Clinical trials for Complication of Surgical Procedure

Safety and Efficacy of XJ-Procedure in Patients With Acute Type A Aortic Dissection Surgery

ADVANCED-XJ-?
Start date: March 1, 2024
Phase: N/A
Study type: Interventional

This is a national, multicenter, open-label, randomized, controlled, endpoint-blinded clinical trial of patients diagnosed with ATAAD and undergoing "Sun's procedure" coordinated by the First Affiliated Hospital of Xi'an Jiaotong University, China. Per the protocol, "Sun's procedure" combined with "XJ-Procedure" in the anastomosis of the aortic root and Sun's procedure combined with regular suturing methods of the aortic root will be compared.

NCT ID: NCT06195267 Not yet recruiting - Aortic Dissection Clinical Trials

Additive Anti-inflammatory Action for Aortopathy & Arteriopathy (Sivelestat) VI

Start date: February 1, 2024
Phase: N/A
Study type: Interventional

Systemic inflammatory response syndrome (SIRS) and multiple organ dysfunction syndrome (MODS) are the major causes of death in patients with acute aortic syndrome (AAS). Therefore, the prevention of SIRS and MODS is of great clinical value, and immunomodulatory therapy with sivelestat may be beneficial. This study was designed to test the hypothesis that the administration of sivelestat during the acute phase of AAS will result in a reduced incidence of SIRS and MODS.

NCT ID: NCT06177548 Not yet recruiting - Aortic Dissection Clinical Trials

Safety and Efficacy of the Minimally Invasive Bentall Procedure Via a Small Right Intercostal Incision in Patients With Aortic Root Lesions

Mini-Bentall
Start date: January 1, 2024
Phase:
Study type: Observational

This study intends to include patients who had aortic root lesions and were treated with Bentall surgery from January 2019 to July 2023 in the First Affiliated Hospital of Xi'an Jiaotong University. The patients will be divided into the minimally invasive group and control group according to the surgical methods: the former underwent minimally invasive Bentall surgery through a small right intercostal incision; the latter underwent traditional Bentall surgery through a median sternal incision. By comparing the clinical data of patients in two groups, we will investigate the effect and safety of minimally invasive Bentall surgery.

NCT ID: NCT06165991 Not yet recruiting - Clinical trials for Postoperative Analgesia

Efficacy and Safety of Liposomal Bupivacaine in Thoracic Paravertebral Nerve Block

Start date: January 1, 2024
Phase: Phase 4
Study type: Interventional

I. Research purpose 1.1 Main Objective: To investigate the efficacy and safety of bupivacaine liposome thoracic paravertebral nerve block combined with drainage tube analgesia for postoperative analgesia after thoracoscopic lobectomy 1.2 Secondary objective: To investigate the efficacy and safety of drainage tube analgesia after thoracoscopic lobectomy 1.3 Exploratory Objective: To investigate the noninferiority of bupivacaine liposomes in thoracic paravertebral nerve block with standard bupivacaine