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Vascular Diseases clinical trials

View clinical trials related to Vascular Diseases.

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NCT ID: NCT03293134 Completed - Clinical trials for Proliferative Vasculopathy

Clinical and Molecular Characterization of Cerebral Proliferative Vasculopathy

VPCA
Start date: July 8, 2013
Phase: N/A
Study type: Observational

As principal objective, the study aims to: 1. Describe the spectrum and evaluate the frequency of angiodysplasia of the nevrax; 2. Establish the physiopathological basis of Fowler's syndrome; 3. Identify FLVCR2 partners and the signaling pathways involved; 4. Test new candidate genes: GPR124 and possible partners of FLVCR2. As second objective, the study aims to: - perform phenotype / genotype correlation if necessary; - and propose a prenatal diagnosis in families with identified mutations.

NCT ID: NCT03280316 Not yet recruiting - Overactive Bladder Clinical Trials

Efficacy Comparison Between Different Management Strategies for Consistent OAB in Patients With SVMs After Surgery

Start date: January 2023
Phase: N/A
Study type: Interventional

The investigators' goal is to compare the efficacy of three different management strategies (sacral neuromodulation, botulinum toxin, M receptor antagonist) in treating consistent OAB in patients with SVMs after surgery.

NCT ID: NCT03280186 Not yet recruiting - Clinical trials for Neurogenic Bladder Dysfunction Nos

Measurement of Bladder Function Change In Patients With SVMs Before and After Surgical Intervention

Start date: January 2022
Phase: N/A
Study type: Interventional

The investigators goal is to create a better understanding of patient with SVMs reported outcomes for bladder management strategies before and after surgery.

NCT ID: NCT03269734 Completed - Clinical trials for Cardiovascular Diseases

Evaluation of the Accuracy of the Vessel Navigator Tool for Catheterization of Supra-aortic Vessels - ARCHIBALD

ARCHIBALD
Start date: December 1, 2018
Phase:
Study type: Observational

This study compares the accuracy of fusion imaging (Fusion Roadmap) versus real-time X-ray imaging (Roadmap) during catheterization of supra-aortic trunks of in patients with aneurysms or arteriovenous malformations.

NCT ID: NCT03264820 Terminated - Vascular Diseases Clinical Trials

Study of the Reproducibility of Laser Measurement in the Detection of Digital Obstructive Arterial Disease (DOAD)

REPROLASER
Start date: December 6, 2017
Phase: N/A
Study type: Interventional

At the digital level, the diagnosis of obstructive arteriopathy is very difficult in the absence of ulcer or of true ischemic signs, and the arteriography, which is an examination to inject an intra-arterial contrast agent, is the reference measure. The measure by "Laser Doppler" uses a monochromatic light (laser) to measure the concentration as well as the speed of travel of red blood cells in the skin and deduct the cutaneous blood flow. The great advantage of this technique is that it is non-invasive, inexpensive and can be performed during a consultation. The patient can therefore be briefly informed of the benign (functional) or organic origin of his disorders.

NCT ID: NCT03253705 Recruiting - Healthy Volunteers Clinical Trials

Samples From Human Subjects to Facilitate Basic, Translational and Clinical Research

Start date: September 14, 2017
Phase:
Study type: Observational

Background: This study is designed to provide samples to help us study the genes your blood cells are making as well as the proteins, sugars, fats, vitamins and other metabolites found in your blood or urine. Blood samples may also be collected to make special cells. These are called induced pluripotent stem cells or iPSCs. Pluripotent stem cells are cells that can be converted into any type of cell. Researchers want to study in the lab iPSCs that are derived from blood samples. Objective: To collect samples to help study genes, proteins, sugars, fats, vitamins, and other metabolites found in blood or urine. Eligibility: Healthy volunteers and patients ages 18 and older Design: First-time research study participants at NIH will have an initial visit for this study that should last no more than 1 hour. All other visits should last 20 30 minutes. Participants will undergo a limited history and physical exam. Participants may have routine blood and urine tests. If participants are giving a blood sample, they must have a hemoglobin level checked in the past 12 months to make sure it is safe for them to give a blood sample for research. Participants may have a venous blood collection. They may do this at several visits. They will lie on a recliner or couch or sit in a chair. A needle will be placed into a vein in the hand or arm, using sterile techniques. Blood will be withdrawn into multiple syringes or tubes. Participants may be asked to provide urine in an appropriate container...

NCT ID: NCT03252925 Completed - Clinical trials for Hematologic Diseases

A Safety and Efficacy Study of NAC in Patients With TA-TMA

Start date: November 1, 2017
Phase: Phase 3
Study type: Interventional

HSCT associated thrombotic microangiopathy(TA-TMA) is a heterogeneous, fatal disorder seen within 100 days post-transplant and presents with thrombocytopenia, hemolysis, acute renal failure, mental status changes and involvement of other organs. N-Acetylcysteine (NAC) is a small, simple molecule that began as a generic drug almost 40 years ago. It has since been approved by the FDA for many indications. The investigators conducted an prospective clinical trial to evaluate the safety and efficiency of NAC in patients with TA-TMA.

NCT ID: NCT03244657 Recruiting - Clinical trials for Polypoid Choroidal Vasculopathy (PCV)

Phase IV Clinical Trial (STAR Study) Extension Study of Conbercept Ophthalmic Injection for Treatment of Polypoid Choroidal Vasculopathy

Start date: April 25, 2017
Phase: Phase 4
Study type: Interventional

To explore efficacy and safety of 0.5 mg conbercept ophthalmic injection for long-term treatment of polypoid choroidal vasculopathy (PCV) subjects.

NCT ID: NCT03241459 Active, not recruiting - Clinical trials for Peripheral Arterial Disease

Safety and Efficacy of the SurVeilâ„¢ Drug-Coated Balloon

TRANSCEND
Start date: October 23, 2017
Phase: N/A
Study type: Interventional

To demonstrate the safety and efficacy of the SurVeil Drug-Coated Balloon (DCB) for treatment of subjects with symptomatic peripheral artery disease (PAD) due to stenosis of the femoral and/or popliteal arteries.

NCT ID: NCT03238222 Recruiting - Clinical trials for Peripheral Arterial Disease

Motivating Structured Walking Activity in Intermittent Claudication

MOSAIC
Start date: November 10, 2017
Phase: N/A
Study type: Interventional

Peripheral arterial disease can cause leg pain or discomfort (called intermittent claudication (IC)), which limits the ability to walk and carry out everyday activities. Lifestyle changes, like increasing walking, can lead to improvements, but can be a challenge to begin and then continue. The aim of this study is to investigate if a physiotherapist-led, behaviour change treatment effects walking in people with IC. The treatment is designed to build an understanding of IC and walking exercise and help individuals develop strategies to increase regular walking. The trial will recruit 192 adults (aged 50 years and over) with IC. All participants will visit King's College London or their local hospital to complete two short walking tests and answer questionnaires about their daily activities, beliefs about their symptoms and treatment, quality of life and the costs of having IC. Participants will then be randomly assigned to receive either the new treatment or continue with their usual NHS care. The new treatment involves two 60-minute face-to-face sessions (at the participant's home or local hospital) and two 20-minute telephone calls with a physiotherapist who will discuss participants' understanding and beliefs about IC, walking and help participants to set goals and plans to increase walking over 12 weeks. Participants will be provided with a step counter (pedometer) and walking record. After 12 weeks, all participants will attend a second appointment where they will repeat the walking tests and fill out another set of questionnaires. A final set of questionnaires will be completed by all participants after 6 months (by post or electronically). Some participants will be invited to provide feedback on their experience of the treatment and trial by telephone or a face-to-face interview with a researcher.