Last updated on April 2019

Registry for Participants With Short Bowel Syndrome


Brief description of study

This is a global prospective, observational, multi-center registry to evaluate the long-term safety profile for participants with short bowel syndrome (SBS) who are treated with teduglutide in a routine clinical setting. The registry will also evaluate the long-term clinical outcomes in participants with SBS. SBS participants treated and not treated with teduglutide will be enrolled.

Clinical Study Identifier: NCT01990040

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Riley Hospital for Children

Indianapolis, IN United States
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Montefiore Medical Center PRIME

Lake Success, NY United States
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Tufts Medical Center

Boston, MA United States
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Global Health Research Center

Miami Lakes, FL United States
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Childrens Hospital of Alabama

Birmingham, AL United States
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Wexner Medical Center

Columbus, OH United States
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Texas Children's Hospital

Houston, TX United States
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UW Digestive Health Center

Madison, WI United States
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Ochsner Health System

New Orleans, LA United States
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Boston Medical Center

Boston, MA United States
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Sanitas Research

Miami, FL United States
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Rigshospitalet

Copenhagen, Denmark
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Henry Ford Health System

Detroit, MI United States
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UCSF Benioff Children's Hospital

San Francisco, CA United States
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Med-Care Research

North Miami Beach, FL United States
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Stony Brook University Hospital

Stony Brook, NY United States
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The Methodist Hospital

Houston, TX United States
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Seattle Children's Hospital

Seattle, WA United States
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Salford Royal

Salford, United Kingdom
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Southampton General Hospital

Southampton, United Kingdom
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St. Mark's Hospital

Harrow, United Kingdom
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Recruitment Status: Open


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