A registry for patients with Short Bowel Syndrome
Research type
Research Study
Full title
A Prospective, Multi-center Registry for Patients with Short Bowel Syndrome
IRAS ID
183578
Contact name
Farooq Rahman
Contact email
Sponsor organisation
NPS Pharmaceuticals, Inc.
Clinicaltrials.gov Identifier
N/A, ENCePP; NCT01990040, Clinicaltrials.gov
Duration of Study in the UK
15 years, 0 months, 31 days
Research summary
This study is a single-group, prospective, observational, multi-centre (ie, world-wide) registry designed to collect data on long-term safety and clinical outcomes in SBS patients. The primary objective of this study is to evaluate the long-term safety profile for patients with short bowel syndrome (SBS)who are treated with teduglutide in a routine clinical setting and secondarily to evaluate long-term clinical outcomes in this patients.
REC name
London - South East Research Ethics Committee
REC reference
15/LO/1564
Date of REC Opinion
19 Oct 2015
REC opinion
Further Information Favourable Opinion