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Found 64,778 clinical trials
A ACHD Research Team

Registry for Mayo Clinic Adult Congenital Heart Disease Control Population

This research study is being done to provide comparative data to the Mayo Clinic Adult Congenital Heart Disease Registry.

18 - 70 years of age All Phase N/A
G Geraldine Liu, MA

Evaluation of Outcome Metrics in Alexander Disease

The purpose of this study is to define the natural history of Alexander Disease, a leukodystrophy that causes neurological dysfunction. Investigators will obtain clinical outcome assessments to measure how the disease affects a patient's gross motor, fine motor, speech and language function, swallowing, and quality of life. Specimens are collected …

years of age All Phase N/A
J Jieqiong Liu

Diagnostic Biomarkers Exploration of Breast Cancer From Serum and Urine

The goal of this observational study is to find the diagnostic biomarkers in serum and urine from early breast cancer patients. The main questions it aims to answer are: compare the different biomarkers in serum and urine from breast cancer patients, benign lesions and healthy population. construct the best diagnostic …

18 - 70 years of age Female Phase N/A
W Wojciech Trzepizur, MD

Microparticles in Obstructive Sleep Apnea

Obstructive sleep apnea (OSA) is independently associated with cardiovascular diseases, including myocardial infarction and stroke. OSA may promote atherosclerosis risk factors such as hypertension, diabetes and dyslipidemia and may have direct proatherogenic effects on the vascular wall. A growing number of studies have recently focused on the role of microparticles …

18 years of age All Phase N/A
L Lidan Jiang, Dr.

Osmotic Therapy for Patients With Severe Subarachnoid Hemorrhage

The goal of this prospective multi-center observational study is to learn about the osmotic therapy in severe subarachnoid hemorrhage (SAH). The main question[s] it aims to answer are: • whether the two osmotic therapy, 20% mannitol and 10% hypertonic saline(HTS), under the same osmotic equivalent, has similar influence on the …

18 - 85 years of age All Phase N/A
A Armine Smith

Mood Alterations in the Patients With Non-Muscle Invasive Bladder Cancer Treated With BCG

The purpose of this study is to evaluate mood changes in patients with Non-Muscle Invasive Bladder Cancer who are receiving intravesical Bacillus Calmete-Guerin (BCG). Patients with Non-Muscle Invasive Bladder Cancer receiving intravesical treatments are eligible to participate in this study. Participation involves providing research blood and urine samples prior to …

18 years of age All Phase N/A
M Mypinder Sekhon, MD PhD

Characterizing the Cerebrovascular Physiology of Circulatory Death During Withdrawal of Life Sustaining Therapies in Humans

The purpose of this study is to better understand what happens in the brain during the dying process. This is a prospective observational study conducted at the end of life in the ICU at VGH. At the time of withdrawal of life sustaining therapies the investigators will monitor brain blood …

19 years of age All Phase N/A
J Jiguang Wang, PhD

Renal Artery Fibromuscular Dysplasia Registry

Study name: A Prospective Study of the Renal artery fibromuscular dysplasia Registry in China Rationale: Fibromuscular dysplasia (FMD) is an idiopathic systemic noninflammatory arterial disease resulting in narrowing of medium-sized arteries. Renal arteries are most commonly involved vessels, although it can also affect arteries in other vascular territories. Renal artery …

years of age All Phase N/A
N Nicole Tovar

Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

The purpose of this research is to understand how to apply cardiac magnetic resonance imaging (CMR) to women with small artery heart disease by looking at the CMRs of women without heart disease. The investigators will study 40 women with no heart disease to learn more about the usefulness of …

35 - 65 years of age Female Phase N/A
A Alice Arapshian

The Severe Von Willebrand Disease (sVWD) Patient Registry

A web-based registry will be created by the sponsor, VWD Connect Foundation (VCF), to collect data on patients with severe Von Willebrand Disease (sVWD). Data will be self-reported by patients and/or collected by registry personnel, as appropriate. The purpose of the sVWD Patient Registry is to create a database of …

years of age All Phase N/A

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