Two-Year test aims to tame debilitating gut condition
NCT ID NCT04881825
Summary
This study is a two-year follow-up to check the long-term safety and continued effectiveness of a weekly injection called glepaglutide for adults with short bowel syndrome (SBS). It includes 129 participants who have already completed a previous trial. The main goal is to monitor for any side effects over a long period while seeing if the treatment keeps helping patients reduce their need for intravenous nutrition.
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Contacts and locations
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Locations
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Asklepios Kliniken Hamburg GmbH
Hamburg, Germany
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Centre Hospitalier Lyon-Sud
Pierre-Bénite, France
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Charité - Universitätsmedizin Berlin
Berlin, Germany
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Georgetown University Medical Center
Washington D.C., District of Columbia, 20007, United States
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Hôpital Beaujon
Clichy, France
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Mayo Clinic College of Medicin
Rochester, Minnesota, 55905, United States
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Norfolk and Norwich University Hospitals
Norwich, United Kingdom
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Rigshospitalet
Copenhagen, Denmark
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St Mark's Hospital
Harrow, United Kingdom
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Szpital Skawina sp. z o.o. im. Stanley Dudricka
Skawina, Poland
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UCLH Foundation NHS Trust
London, United Kingdom
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UMC Radboud Nijmegen
Nijmegen, Netherlands
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Universitair Ziekenhuis Leuven
Leuven, Belgium
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University of Nebraska Medical Center
Omaha, Nebraska, 68198, United States
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Universitätsklinikum Bonn
Bonn, 53127, Germany
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Universitätsklinikum Frankfurt
Frankfurt, Germany
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Universitätsmedizin Rostock
Rostock, Germany
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Vanderbilt University Medical Center, Nashville
Nashville, Tennessee, 68198-3285, United States
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Wojewodzki Specjalistyczny Szpital im. M. Pirogowa w Lodzi
Lodz, Poland
Conditions
Explore the condition pages connected to this study.