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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 |