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Malabsorption Syndromes clinical trials

View clinical trials related to Malabsorption Syndromes.

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NCT ID: NCT03168555 Completed - Cholelithiasis Clinical Trials

Changes in Bile Acid Homeostasis and Stool Habits After Cholecystectomy

BACH
Start date: June 22, 2017
Phase: Phase 4
Study type: Interventional

Investigate serial plasma samples of fibroblast growth factor 19 (FGF19) after oral stimulation with chenodeoxycholic acid in the same subjects before and after elective cholecystectomy

NCT ID: NCT03140371 Completed - Malnutrition Clinical Trials

High Energy High Protein Peptide Feed Study

Start date: July 14, 2017
Phase: N/A
Study type: Interventional

Oral nutritional supplements and enteral tube feeds are commonly used to meet the nutritional requirements of patients with disease-related malnutrition, or who require medical nutrition support for other reasons. Some patients may not tolerate standard formulations containing whole proteins (typically due to maldigestion/malabsorption) leading to gastrointestinal symptoms (i.e. vomiting and diarrhoea). Without appropriate management, this may lead to reduced nutritional intake, increased nutritional losses and risk of malnutrition in patients who may already have elevated nutritional requirements due to their clinical conditions. Poor tolerance to standard feed formulations can be managed with extensively hydrolysed (peptide-based) enteral feeds, where the protein source is provided in smaller proteins. Patients with elevated nutritional requirements, poor tolerance, maldigestion and/or malabsorption often require a higher energy, higher protein feed to meet their nutritional requirements in a smaller volume of feed. The study feed is a high energy (1.5kcal/ml), high protein (7.5g protein/100ml) peptide-based feed, available as a 500ml enteral tube feed, and a 200ml Vanilla-flavour oral nutritional supplement. The study will investigate the gastrointestinal tolerance, compliance and acceptability of the high energy, high protein peptide-based feed in 60 adult patients requiring a peptide-based feed, in several NHS sites across England. Patients will be asked to take the study feed for 28 days. Data will be recorded using questionnaires with no invasive measures. The primary outcome is gastrointestinal tolerance with secondary outcomes of compliance, acceptability, nutrient intake and anthropometry.

NCT ID: NCT03138902 Completed - Clinical trials for Carbohydrate Intolerance

Carbohydrate Intolerance Questionnaire Study

Curves1
Start date: June 1, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the validity of using a carbohydrate intolerance questionnaire (CIQ) and/or other health markers as a means of predicting response to insulin sensitivity as determined by an oral glucose tolerance test (OGTT).

NCT ID: NCT03059537 Completed - Clinical trials for Bile Acid Malabsorption

Validation of Stimulated ∆FGF19 for Diagnosing Bile Acid Diarrhoea

VABAD
Start date: March 13, 2017
Phase: Phase 4
Study type: Interventional

This study aims to validate a possible diagnostic test for bile acid diarrhoea prospectively compared to the SeHCAT scintigraphy. Fasting participants are given a standard meal and 1,250 mg chenodeoxycholic acid. The investigators measure fasting FGF19, bile acids species including 7-alpha-CHO and serial blood samples after the stimulation.

NCT ID: NCT03011593 Completed - Ulcerative Colitis Clinical Trials

Effect of UGIR in Adults With Compromised Gut Function and Malabsorption

Start date: November 2015
Phase: N/A
Study type: Interventional

This study assessed the effect of a nutrition support product on quality of life in adults with compromised gut function and malabsorption.

NCT ID: NCT03009916 Completed - Clinical trials for Bileacid Malabsorption

Bileacid Malabsorption and GLP-1 Secretion

Start date: March 2016
Phase: Phase 4
Study type: Interventional

The aim of this study is to examine the influence of BAM on postprandial GLP--1 secretion and glucose homeostasis, both with and without bile acid sequestration.

NCT ID: NCT02987569 Completed - Malnutrition Clinical Trials

Teen and Young Adult Connections for Support From Multidisciplinary Professionals & Peers

Start date: July 2016
Phase: N/A
Study type: Interventional

12 month study testing mobile delivery of health information and connections to professionals and peers to improve health of teen/young adult HPN users.

NCT ID: NCT02953223 Completed - Clinical trials for Short Bowel Syndrome

A Study to Monitor the Use of an Amino Acid-Based Infant Formula

EAGLE
Start date: January 2017
Phase:
Study type: Observational [Patient Registry]

To assess the frequency and nature of adverse events in infants fed a free amino acid based infant formula.

NCT ID: NCT02849704 Completed - Clinical trials for Chronic Pancreatitis

Fat Malabsorption in Chronic Pancreatitis

Start date: October 13, 2016
Phase: Phase 2
Study type: Interventional

The objective of this study is to evaluate the malabsorption blood test (MBT), stool coefficient of fat absorption (CFA) and stool bomb calorimetry (BC) methods as potential screening or diagnostic tests for reduced exocrine pancreatic function or pancreatic insufficiency (RPF/PI). A further objective is to determine the test responses before and after pancreatic enzyme medication administration (Creon36™) in the patients with chronic pancreatitis (CP).

NCT ID: NCT02798718 Recruiting - Clinical trials for Cardiovascular Disease

Whole Milk Intake and Cardio-metabolic Risk Factors

Start date: May 2016
Phase: N/A
Study type: Interventional

Milk is the source of high-quality protein, calcium, and other vitamins and minerals. Epidemiologic studies have linked high consumption of milk with risk of metabolic syndrome, T2DM, hypertension and obesity, which are independent risk factors of cardiovascular disease. However, milk contains disaccharide lactose, which may cause gastrointestinal problems in those adults with poor digestion. Recent studies have shown that subjects with intolerance to lactose tend to reduce their consumption of milk. Actually, consumption of 12g lactose (240ml milk) per day produces negligible symptoms in lactose intolerant. Furthermore, a dairy-rich diet could improve lactose intolerance because of colonic adaption to it. Lactose maldigestion would not be a restricting factor in milk intake. In general, the undigested lactose will be fermented by colonic bacteria into hydrogen, carbon dioxide, and short-chain fatty acids (SCFA: acetate, propionate, and butyrate). The SCFAs may have beneficial effects on human glucose and lipid metabolism, and the lactose fermentation may change the intestinal flora profile. But there are few studies evaluating effect of milk intake on health of people with lactose malabsorption or intolerance.This trial intend to study the effect of whole milk on cardio-metabolic risk factors of healthy person with or without lactose maldigestion.