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Vascular Diseases clinical trials

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NCT ID: NCT05524896 Completed - Vascular Diseases Clinical Trials

Elucidate Vasodilatory Capacity From Histology-Defined Analysis of Coronary CT Angiography

HD-FFRct
Start date: January 1, 2017
Phase:
Study type: Observational

Coronary CT Angiography (CCTA) may be an ideal modality to fill gaps in understanding the extent and rate of progression coronary artery disease. The investigators have developed an image analysis software ElucidVivo that estimates relevant indices, including fractional flow reserve (FFR) . In this study, the investigators aim to assess the value of ElucidVivo-based plaque morphology characterization for predicting non-invasive FFR in patients with suspected coronary artery disease (CAD) who had undergone clinically indicated coronary CTA and invasive coronary angiography (ICA) for physical FFR measurement.

NCT ID: NCT05485467 Completed - Clinical trials for Heart Transplant Failure

The Role of CD34 + Stem Cells and Biomarkers in the Development of CAV in HTX Patients

Start date: June 1, 2022
Phase:
Study type: Observational

Coronary allograft vasculopathy represents one of the major limiting factors of long-term survival in heart transplant recipients. While extensively researched, the underlying mechanisms of coronary allograft vasculopathy (CAV) after heart transplantation remain incompletely understood. As CD34+ cells represent one of the key determinants of coronary vascular homeostasis we investigated the potential association between CAV and CD34+ cell count in heart transplant recipients.

NCT ID: NCT05388409 Completed - Clinical trials for Porto-Sinusoidal Vascular Disease

Risk Factors for Portosinusoidal Vascular Disease in Kidney Transplant Recipients:

TRANSVAS
Start date: October 25, 2021
Phase:
Study type: Observational

To look for the factors of exposure present prior to the onset of Porto-Sinusoidal Vascular Disease (PSVD) and which can lead to the occurrence of PSVD after renal transplantation, and therefore to consider the identification of risk factors, in order to prevent or detect early signs of portal hypertention in predisposed patients and improve their prognosis.

NCT ID: NCT05373108 Completed - Clinical trials for Cardiac Allograft Vasculopathy

Endothelin-1 and Cardiac Allograft Vasculopathy (CAV)

Start date: May 19, 2022
Phase: Phase 4
Study type: Interventional

Many patients with end-stage heart failure, a condition in which the heart fails to pump enough blood to support the body's other organs, are fortunate enough to receive a heart transplant. However, despite taking medicines aimed at blunting the immune system's response to the donor heart, some of them will develop transplant-related disease in the coronary arteries supplying their hearts. Fifty years after the first human-to-human heart transplant, this disorder-cardiac allograft vasculopathy (CAV)-remains a leading cause of long-term death and has been coined the 'Achilles' Heel' of heart transplantation. Indeed, a better understanding of how CAV occurs and improved therapies to prevent and/or slow its development are desperately needed to meaningfully impact patient outcomes. Endothelin-1 (ET-1) is a key molecular regulator of arterial health, and our prior data suggests that it is associated with accelerated CAV. In this particular study of recent heart transplant recipients, we are asking: Does ET-1 contribute to the coronary artery's capacity to dilate/constrict? To answer this question, during the cardiac catheterization at 1 year post-transplant (standard of care), we will measure blood levels of ET-1 and perform an invasive evaluation of coronary vasomotor function inn a consecutive subset of patients who will have received a 1-week course of the oral endothelin receptor antagonist (macitentan) prior this catheterization, which will allow us to test how much ET-1 contributes to coronary responsiveness. The findings from this study may provide the necessary foundation to study whether endothelin receptor antagonists are able to effectively reduce the rate of accelerated CAV.

NCT ID: NCT05337644 Completed - Obesity, Morbid Clinical Trials

Indocyanine Green Test for Evaluation of Perfusion of Staple Line of the Stomach During Laparoscopic Sleeve Gastrectomy

Start date: January 21, 2022
Phase:
Study type: Observational

The investigators present the case of a 40-year-old female underwent laparoscopic sleeve gastrectomy. Intraoperative indocyanine green test was performed

NCT ID: NCT05296031 Completed - Vascular Diseases Clinical Trials

Drug Eluting Stent Zilver PTX vs Bare Metal Stent Zilver Flex

Start date: March 1, 2013
Phase: N/A
Study type: Interventional

Randomized study comparing the results between drug-eluting stents and standard bare metal stents, when treating femoropopliteal lesions in patients with critical limb ischemia.

NCT ID: NCT05253521 Completed - Diabetes Clinical Trials

The Role of South Asian vs European Origins on Circulating Regenerative Cell Exhaustion

ORIGINS-RCE
Start date: January 8, 2022
Phase:
Study type: Observational

ORIGINS-RCE is an observational, cross-sectional, two-arm study aimed at determining if an individual's ethnic origin influences the number of blood vessel-forming stem cells in the bloodstream. Circulating progenitor cells will be enumerated and the distribution patterns of these cell types will be assessed to determine if these parameters differ between individuals of South Asian origin and European origin. Specifically, this study will evaluate if differential regenerative cell exhaustion (RCE) may account, at least in part, for the differences in cardiovascular risk reported between individuals of South Asian vs European origin.

NCT ID: NCT05247944 Completed - Vascular Diseases Clinical Trials

F-BEVAR vs Open Surgery for Complex Abdominal Aortic Aneurysm

Start date: January 2010
Phase:
Study type: Observational

The aim of the present study was to investigate outcomes of a propensity matched series of patients treated with F-BEVAR and open surgery repair for complex abdominal aortic aneurysm in two aortic high-volume centres.

NCT ID: NCT05229237 Completed - Clinical trials for Polypoidal Choroidal Vasculopathy

Conbercept for Polypoidal Choroidal Vasculopathy(START Study)

Start date: May 1, 2018
Phase:
Study type: Observational [Patient Registry]

1. To evaluate the effectiveness of Conbercept for PCV patients. 2. To describe the characteristics of PCV. 3. To describe the adverse events (AE) of Conbercept in the treatment of PCV. 4. Todescirbe the real situation and prognosis of PCV patients in our country.

NCT ID: NCT05199792 Completed - Vascular Diseases Clinical Trials

Efficacy of Gadoterate Meglumine in Diagnosis of Vascular Diseases Using MRA MRA

Start date: June 2, 2017
Phase:
Study type: Observational

The purpose of this study is to compare magnetic resonance angiography (MRA) using gadoterate meglumine to clinically obtained MRA using gadobutrol. The specific aims are to show: 1. Carotid, chest, and abdomenal MRA with gadoterate meglumine has a comparable image quality and diagnostic confidence to MRA using gadobutrol. 2. Carotid, chest, and abdomenal MRA with gadoterate meglumine has a comparable accuracy for vascular lesion and stenosis detection compared to MRA using gadobutrol.