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Gastric Emptying clinical trials

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NCT ID: NCT03239821 Completed - Healthy Clinical Trials

Clinical Evaluation of the VIPUN Balloon Catheter 0.1

ANTERO-1
Start date: September 25, 2017
Phase: N/A
Study type: Interventional

The primary aim of this investigation is to assess the safety, feasibility and performance of the VIPUN Balloon Catheter 0.1 in the assessment of gastric motility. The investigation will also assess whether the inflation of the VIPUN Balloon Catheter can stimulate gastric motility and emptying. Furthermore, this investigation will examine whether gastric motility and emptying as measured in this study are correlated.

NCT ID: NCT02938065 Completed - Gastric Emptying Clinical Trials

Gastric Emptying Ultrasound Research Study

GERS
Start date: June 2016
Phase: N/A
Study type: Interventional

The proposed study will use this technology to observe emptying of the stomach of a protein and carbohydrate rich clear liquid sports/nutrition drink.

NCT ID: NCT02735889 Completed - Gastric Emptying Clinical Trials

Fizzy Drinks Study

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

The objective of this study is to compare the effect of different levels of carbonation isocaloric beverages on glycemic response (using protocol based on standardized glycemic index testing methodology), gastric emptying and satiety. It is hypothesized that carbon dioxide will delay gastric emptying, and in turn, attenuate glycemic response and enhance satiety. The use of a non-nutrient (gas) in improving glycemic response and satiety would have important health implications for the beverage industry.

NCT ID: NCT02665923 Recruiting - Gastric Emptying Clinical Trials

Gastric Emptying in Neonates and Infants After Formula Feeding

Start date: March 2016
Phase:
Study type: Observational

Ultrasound imaging will be used to evaluate time for gastric emptying in healthy, fasting newborns, and infants following feeding of clear liquids and/or milk (including breast or formula).

NCT ID: NCT02587611 Completed - Gastric Emptying Clinical Trials

Randomized Comparison of Elemental Liquid Diet and Standard Semi-solid Diet on Gastric Emptying

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

The purpose of this study is to compare the effect of either elemental liquid diet or standard semi-solid diet on gastric emptying in both healthy subjects and bedridden patients receiving gastrostomy feeding.

NCT ID: NCT01809938 Completed - Gastric Emptying Clinical Trials

Does Adding Milk to Tea Delay Gastric Emptying?

GETEAM
Start date: November 2011
Phase: N/A
Study type: Interventional

Most pre-operative fasting regimes dictate that if there is any milk added to tea or coffee, the preoperative fasting time should be extended from 2 to 6 hours. The purpose of this study is to demonstrate whether there is really a delay in gastric emptying time associated with the inclusion of milk in a cup of tea.

NCT ID: NCT01635491 Completed - Gastric Emptying Clinical Trials

Gastrointestinal Transit Times and Motility in Healthy Volunteers Obtained by Motilis-3D-transit

Start date: April 2012
Phase: N/A
Study type: Observational

The purpose of this study is to describe gastrointestinal motility and transit times in healthy subjects by using Motilis 3D-Transit and to compare the total gastrointestinal transit time (GITT) to GITT obtained using radioopaque markers. The investigators end points are to measure the transit times through different segments of the gastrointestinal canal,e.g. gastric emptying, small intestine, total GITT. The study is descriptive and is designed to test and evaluate the usefulness of the Motilis 3D-Transit system. The investigators hypothesize, that with the system transit times through different segments of the gastrointestinal canal can be measured. The design is made for evaluating the transit times, the inter-subject reproducibility and comparison with gold standard for colonic transit time measurement. The investigators have chosen to include 20 healthy volunteers.The study is descriptive and therefore power calculation is not needed.

NCT ID: NCT01350284 Completed - Diabetes Mellitus Clinical Trials

The Effect of Natural Food Flavourings on Gastrointestinal and Cardiovascular Physiological Responses.

CinnGastEmpt
Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether 3 g cinnamon was sufficient to delay the gastric emptying rate of a high-fat solid meal and subsequently reduce postprandial blood glucose and lipid responses, oxidative stress, arterial stiffness and satiety responses in a healthy adult population.

NCT ID: NCT01226134 Recruiting - Clinical trials for Functional Dyspepsia

Effect Of Itopride On Gastric Emptying And Accommodation In Patients With Functional Dyspepsia

EIGEAPFD
Start date: February 2009
Phase: N/A
Study type: Interventional

Pathogenesis of functional dyspepsia is poorly understood. Gastrointestinal motor abnormalities, Helicobacter pylori infection, impaired gastric accommodation to a meal, hypersensitivity of the afferent nerves of the gut, psychological disturbances and central nervous system dysfunction have been proposed. Pharmacological treatments for patients with functional dyspepsia remain unsatisfactory. Only small benefits relative to placebo have been found with histamine H2 receptor antagonists, proton pump inhibitor and Helicobacter pylori eradication. Itopride is a dopamine antagonist with acetylcholinesterase inhibitory actions. This agent is currently indicated for patients with various upper GI symptoms. This study is aimed to evaluate the effect of Itopride on gastric emptying(by 13-C Octanoic acid breath Test), accommodation (by Gastric Scintigraphy SPECT and slow nutrient drinking test)and symptoms in FD patients

NCT ID: NCT01139216 Completed - Clinical trials for Functional Constipation

Effect of TU-100 on Rectal Compliance, Rectal Sensation and Small Bowel and Colonic Transit in Females With Constipation

Start date: August 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess the dose-related effects of TU-100, a botanical agent that modulates gastrointestinal nerves, on rectal compliance, rectal sensation thresholds and small bowel and colonic transit in female patients with functional constipation as compared to placebo.