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Aneurysm, Dissecting clinical trials

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NCT ID: NCT03669055 Recruiting - Aortic Dissection Clinical Trials

Hemodynamic Changes in the Aorta After Endovascular Treatment of the Aortic Dissection

4DAo
Start date: March 7, 2019
Phase: N/A
Study type: Interventional

Aortic dissection (AD) is a serious pathology affecting one person for 300 000 habitants per year. In case of complicated AD on the descending aorta, it is necessary to perform an endovascular surgery in association with medical treatment. An endoprosthesis is implanted on the descending thoracic aorta in order to close the main intimal tear. This closure lead to an increase in the thoracic true lumen diameter, a decrease in the thoracic false lumen diameter, a better perfusion of the aortic branches. Furthermore, even in case of open surgical treatment of the ascending aorta it can be necessary to perform an endovascular treatment on the descending aorta, either to prevent and treat aneurysmal evolution or to treat patent malperfusion syndrome. CT and Magnetic Resonance angiography, by the realization of an aortic morphologic evaluation, are the two key imaging exams in the DA. Nevertheless, CT can't provide aortic dynamic evaluation, contrary to MRI. This exam, thanks to the phase-contrast sequence can measure velocity and flow data in vessels, including aorta but also true and false lumen in the AD. Thus, by verifying the perfusion of the aortic true lumen and the aortic branches it is possible to perform an early evaluation of the endovascular treatment of the DA. Actually, only one study has realized an aortic dynamic evaluation on the AD, unfortunately this study was limited to non-operated patients. In order to assess the place of MRI in the AD, the ingestigation propose to determine if phase-contrast MRI is able to evaluate the impact of the endovascular treatment on the hemodynamic state of the aorta and its branches.

NCT ID: NCT03647566 Completed - Aortic Dissection Clinical Trials

18F Sodium Fluoride PET/CT in Acute Aortic Syndrome

FAASt
Start date: October 1, 2018
Phase:
Study type: Observational

The purpose of this study is to determine whether Sodium Fluoride imaging (using Positron Emission Tomography-Computed Tomography - PET-CT) is able to predict disease progression in acute aortic syndrome.

NCT ID: NCT03607981 Recruiting - Clinical trials for Spontaneous Coronary Artery Dissection

Spanish Registry on Spontaneous Coronary Artery Dissection

SR-SCAD
Start date: January 1, 2015
Phase:
Study type: Observational [Patient Registry]

Multicenter observational prospective registry, Spanish nationwide-based, of consecutive patients diagnosed with Spontaneous Coronary Artery Dissection (SCAD)

NCT ID: NCT03607786 Recruiting - Hypothermia Clinical Trials

Antegrade Cerebral Perfusion and Retrograde Inferior Vena Caval Perfusion for Total Aortic Arch Replacement

CARTAR
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

This study is designed as a multicenter, randomized, assessor- blinded clinical trial.The primary aim of this trial is to assess whether retrograde inferior venal caval perfusion combined selective antegrade cerebral perfusion(ACP)under mild hypothermia, compared with moderate hypothermia combined with selective ACP alone, improves the outcome for the patients undergoing total aortic arch replacement.

NCT ID: NCT03552848 Recruiting - Clinical trials for Multiple Organ Dysfunction Syndrome

Mesenchymal Stem Cells for Multiple Organ Dysfuntion Syndrome After Surgical Repaire of Acute Type A Aortic Dissection

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

Multiple organ dysfunction syndrome (MODS) after surgical repaire for acute type A aortic dissection(ATAAD) is a life-threatening condition. In this study, patients who undergoing surgical repaire of ATAAD immdediately or presenting sever MODS after surgical repaire of acute type A aortic dissection will be treated with umbilical cord-derived mesenchymal stem cell.

NCT ID: NCT03530748 Recruiting - Aortic Dissection Clinical Trials

On-table Renal Perfusion Evaluation Renal Artery Stenosis or Obstruction

Start date: April 9, 2018
Phase:
Study type: Observational

1. Evaluate the feasibility for the on-table evaluation of the renal perfusion by using Syngo Dyna Parenchymal Blood Volume(PBV) Body; 2. Explore the clinical benefits of this application during procedure to help the physician to determine the procedure endpoint.

NCT ID: NCT03479736 Completed - Retinal Detachment Clinical Trials

A Study of Fluoroquinolones Exposure and Collagen-Related Serious Adverse Events

Start date: November 20, 2017
Phase:
Study type: Observational

The purpose of this study is to evaluate whether there is an increased risk of achilles tendon rupture (ATR), retinal detachment (RD) or aortic aneurysm and dissection (AAD) following exposure to fluoroquinolone (FQ) or other antibiotics (amoxicillin, azithromycin, trimethoprim and trimethroprim/sulfamethoxazole) or febrile illness not treated with antibiotics, using a study design that minimizes the impact of confounders not usually captured in health services databases such as heredity or smoking.

NCT ID: NCT03435159 Completed - Neck Pain Clinical Trials

Effects of Spinal Manipulation on Vertebrobasilar and Internal Carotis Arteries in Healthy Population

Start date: February 17, 2017
Phase: N/A
Study type: Interventional

After lumbar pain, neck pain is the most common cause of patients needing chiropractic care; the second most common cause of spinal manipulation use (1). Manipulation and mobilization are commonly used by chiropractors, osteopaths and manipulative physiotherapists in the treatment of neck pain. Many studies show that the Activator instrument is also used for this purpose in the chiropractic profession (2) There are several published case reports that relate to neck manipulation to vertebral artery dissection and stroke. The prevailing theory is that the neck extension and / or rotation may damage the vertebral artery in the foramen transversarium, especially at the C1-C2 level (2). However, most cases of extracranial vertebral artery dissection are thought to be spontaneous (3). In the literature, there have been no studies investigating the effects of instrument-assisted spinal manipulation on vertebrobasilar and internal carotis arteries. the aim of this study to compare the effect of manual and instrumental spinal manipulation on blood flow parameters of vertebrobasilar and internal carotis arteries on healthy persons which have mechanical neck pain and asymptomatic in vertebrobasilar insufficiency test.

NCT ID: NCT03398850 Recruiting - Clinical trials for Coronary Artery Dissection, Spontaneous

Spontaneous Coronary Artery Dissection anaLysIs of the Brazilian Updated Registry

SCALIBUR
Start date: January 1, 2000
Phase: N/A
Study type: Observational [Patient Registry]

A retrospective and prospective registry will evaluate demographic and angiographic data in patients with spontaneous coronary artery dissection (SCAD) using medical records, invasive coronary angiography, intravascular imaging and/or computed multislice coronary tomography. The type of treatment applied during index hospitalization (i.e., clinical management, percutaneous coronary intervention or coronary artery bypass grafting) will be evaluated. Long-term follow-up (up to 10 years) will be also reported.

NCT ID: NCT03390998 Completed - Clinical trials for Spontaneous Coronary Artery Dissection

Angiographic and Psychosocial Evaluation of Peripartum vs. Non: SCAD

SCAD
Start date: November 28, 2017
Phase:
Study type: Observational

This multi-site international clinical research project is a collaboration between investigators from multiple institutions in the USA, Canada, and Europe. Approximately 7 to 11 sites will participate and provide data for analysis. Clinical operations (for data collection and analysis) across sites will be managed by Stanford. The study purpose is to determine differences in clinical and imaging presentation, in-hospital management and prognosis in peripartum and non-peripartum SCAD patients.