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Rare and Atypical Diabetes Network
University of South Florida
Diabetes Mellitus
Diabetes Mellitus Progression
Glucose Intolerance
Glucose Metabolism Disorders
Metabolic Disease
RADIANT is a network of 14 clinical sites and several laboratories dedicated to the study
of atypical diabetes.
The objective of this study is to define new forms of diabetes and the unique mechanisms
underlying these forms of atypical diabetes. The specific aims are to:
1. Identify and enroll1 expand
RADIANT is a network of 14 clinical sites and several laboratories dedicated to the study of atypical diabetes. The objective of this study is to define new forms of diabetes and the unique mechanisms underlying these forms of atypical diabetes. The specific aims are to: 1. Identify and enroll individuals and families with undiagnosed rare and atypical forms of diabetes. 2. Determine the etiologic basis of the metabolic disorder among individuals and families with novel forms of rare and atypical diabetes. 3. Understand the pathophysiology of individuals and families with novel forms of rare and atypical forms of diabetes. Type: Observational Start Date: Sep 2020 |
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Cardiopulmonary Bypass Induced Red Blood Cell Lysis
University of Maryland, Baltimore
Cardiopulmonary Bypass
Cardiac Surgery
Kidney Injury, Acute
Studying the dynamics of red blood cell lysis, pfH, protective proteins and organ injury,
limits will be set for safe levels of pfH following the use of CPB. These results will be
compared to existing laboratory-based methods for determining red blood cell damage to
predict CPB assist device safety1 expand
Studying the dynamics of red blood cell lysis, pfH, protective proteins and organ injury, limits will be set for safe levels of pfH following the use of CPB. These results will be compared to existing laboratory-based methods for determining red blood cell damage to predict CPB assist device safety. Further, results from the studies described in this proposal will help develop therapeutic strategies to benefit patients by early detection of pfH and clearance protein levels that occur during CPB. Type: Observational Start Date: Mar 2022 |
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CVD 38000: Study of Responses to Vaccination With Typhoid and/or Cholera
University of Maryland, Baltimore
Typhoid and/or Cholera Vaccination
This is an open-label, non-randomized study. The purpose of this study is to better
understand how vaccines against typhoid fever and cholera affect the normal immune system
and bacteria in the intestine. Patients having standard-of-care endoscopies (colonoscopy
and/or esophagogastroduodenoscopy (E1 expand
This is an open-label, non-randomized study. The purpose of this study is to better understand how vaccines against typhoid fever and cholera affect the normal immune system and bacteria in the intestine. Patients having standard-of-care endoscopies (colonoscopy and/or esophagogastroduodenoscopy (EGD)) will be divided into 3 groups: Group 1: Vivotif typhoid vaccination and/or Vaxchora cholera vaccination then endoscopy Group 2: Endoscopy, then Vivotif typhoid vaccination and/or Vaxchora cholera vaccination, then follow-up endoscopy Group 3: Endoscopy without vaccination. Both vaccines used in this study are licensed by the Food and Drug Administration (FDA) for travelers to developing countries. Volunteers will be asked to donate tissue, blood, saliva and stool samples for studying how the body responds to the typhoid and/or cholera vaccine. Type: Interventional Start Date: Nov 2018 |
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Spinal Cord Injury Registry - North American Clinical Trials Network
Robert G. Grossman, MD
Spinal Cord Injury
The NACTN Spinal Cord Injury Registry is a network of clinical centers collecting
de-identified data from patients admitted through the Emergency Department of a NACTN
center at the time of injury with an initial (first time) spinal cord injury (SCI).
Information will be collected on the natural hi1 expand
The NACTN Spinal Cord Injury Registry is a network of clinical centers collecting de-identified data from patients admitted through the Emergency Department of a NACTN center at the time of injury with an initial (first time) spinal cord injury (SCI). Information will be collected on the natural history of SCI and course of treatment through the first 12 months from the date of injury or long as medically indicated. Data collected includes imaging information from CT or MRI scans, neurological and general medical outcome and rehabilitation evaluation. No intervention is given other than standard of care for spinal cord injury, intensive monitoring and frequent follow up care. Type: Observational Start Date: Jul 2005 |