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Short Bowel Syndrome clinical trials

View clinical trials related to Short Bowel Syndrome.

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NCT ID: NCT04857801 Completed - Clinical trials for Short Bowel Syndrome

Teduglutide in Short Bowel Syndrome Patients

Start date: June 1, 2016
Phase:
Study type: Observational

A retrospective analysis was performed using data of patients suffering from non-malignant SBS-IF. They were treated with teduglutide in a multidisciplinary SBS-IF program at a single university medical center between June 2016 and June 2020.

NCT ID: NCT04832087 Completed - Clinical trials for Short Bowel Syndrome

Pediatric Teduglutide Registry

PTR
Start date: May 18, 2021
Phase:
Study type: Observational [Patient Registry]

Pediatric specific post-marketing registry to evaluate the long-term safety and efficacy of teduglutide.

NCT ID: NCT04775706 Recruiting - Clinical trials for Short Bowel Syndrome

Phase 2 Study to Assess the Safety, PK, and PD in SBS-IF Subjects

Start date: March 3, 2022
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blind, placebo-controlled, proof-of-concept (PoC), Phase 2 study to assess the safety, PK, and PD of SC administration of HM15912 in adult subjects with SBS-associated intestinal failure (SBS-IF).

NCT ID: NCT04743960 Completed - Sleep Clinical Trials

Assessing Metabolic and Sleep Consequences of Overnight Home Parenteral Nutrition

Start date: October 5, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether advancing the timing of home parenteral nutrition from overnight to daytime regimens leads to improved glucose profiles and sleep quality, and other changes in plasma metabolic signatures.

NCT ID: NCT04733066 Recruiting - Clinical trials for Short Bowel Syndrome

Quality of Life in Patients With Short Bowel Syndrome Treated Without and With Teduglutide - a Prospective Nested Matched Pair Analysis

MatchedQoL
Start date: September 1, 2020
Phase:
Study type: Observational

The aim of this prospective longitudinal study is to compare the quality of life of short bowel patients prior to and on teduglutide treatment with a non-treated patient group in a matched-pair design.

NCT ID: NCT04627025 Completed - Clinical trials for Short Bowel Syndrome

Trial to Evaluate Efficacy and Safety of Apraglutide in SBS-IF

STARS
Start date: January 26, 2021
Phase: Phase 3
Study type: Interventional

The primary objective of the trial is the confirmation of the efficacy of apraglutide to evaluate the efficacy of weekly subcutaneous apraglutide in reducing parenteral support dependency.

NCT ID: NCT04604275 Recruiting - Short Gut Syndrome Clinical Trials

Functional Sucrase Deficiency in Short Bowel Syndrome Patients With Intestinal Failure

Start date: February 2, 2022
Phase: Phase 2
Study type: Interventional

Short gut syndrome with intestinal failure patients may have decreased production of disaccharidases, like sucrase, an enzyme responsible for digesting sugar in foods. This can happen due to loss of bowel length from surgery or from loss of cellular function in the intestines due to use of parenteral nutrition intravenously. Therefore, patients with these conditions may not be able to digest sucrose (sugar) fully. Patients might experience abdominal distension/pain, vomiting and diarrhea when sugar is taken in orally or through the g-tube, which can limit patients' ability to increase oral or g-tube feeds in short gut syndrome patients with intestinal failure. In patients with short gut syndrome and intestinal failure, the administration of exogenous sucrase (enzyme) may improve sucrose (sugar) digestion and thus the ability to tolerate more oral or g-tube feeds.

NCT ID: NCT04522778 Active, not recruiting - Quality of Life Clinical Trials

Innovative Central Line Securement Device in the Pediatric Population

Start date: November 5, 2020
Phase: N/A
Study type: Interventional

This study involves evaluating pediatric patients with central lines to determine differences in line complications and quality of life in those with a novel central line securement device (wrap) as compared to those who use a traditional securement device (dressing).

NCT ID: NCT04474743 Completed - Clinical trials for Chronic Pancreatitis

Malnutrition in Chronic Gastrointestinal Diseases, Cross-sectional Study

Start date: October 2, 2018
Phase:
Study type: Observational

Malnutrition and muscle wasting are common consequences of life-threatening, chronic diseases of the gastrointestinal tract. Such diseases include liver cirrhosis, chronic pancreatitis and short bowel syndrome. Malnutrition and muscle wasting increase the risk of complications, reduce the life expectancy and impair the quality of life. The development of malnutrition and muscle wasting is different, as is the diagnosis and nutritional treatment. There are also different mechanisms of origin for the underlying diseases. The aim of the study is to compare data related to nutrition and physical condition of patients with liver cirrhosis, chronic pancreatitis and short bowel syndrome. Malnutrition and muscle wasting within the specific diseases will be characterized and possible correlations will be identified. For this, malnourished and non-malnourished patients of the different diseases are compared with controls patients with non-specific complaints of the gastrointestinal tract as well as with healthy study participants. Data on food intake, physical activity, body composition and body measurements as well as muscle strength and muscle function are recorded. Blood values as well as transport and barrier properties of the intestine will also be examined.

NCT ID: NCT04450472 Completed - Clinical trials for Short Bowel Syndrome

Nonthyroidal Illness Syndrome in SBS

Start date: December 31, 2016
Phase:
Study type: Observational

Nonthyroidal illness syndrome (NTIS) is prevalent in critical illness; it is associated with poor outcomes. However, few studies have focused on the relationship between NTIS and short bowel syndrome (SBS). The aim of this study was to investigate the incidence, etiology, and prognosis of NTIS and its correlation in clinical variables in adult patients with SBS.