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Gastric Emptying clinical trials

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NCT ID: NCT05641051 Completed - Clinical trials for Randomized Controlled Trial

Metoclopramide on Gastric Emptying in Mechanically Ventilated Patients

Start date: December 14, 2022
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the prokinetic effect of metoclopramide on gastric emptying in critically ill mechanically ventilated patients .

NCT ID: NCT05555407 Completed - Gastric Emptying Clinical Trials

Feasibility of a Wireless Patch System (WPS) to Measure Gastrointestinal Motility and Gastric Emptying

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the utility of a new device - an external wireless patch system (WPS) - to measure gastric motility and to compare this external wearable device with the most commonly used test to measure stomach emptying, the nuclear medicine gastric emptying scan (also called gastric scintigraphy).

NCT ID: NCT05333237 Completed - Gastric Emptying Clinical Trials

Gastric Emptying of High Calorie Liquid Meals

Start date: March 28, 2022
Phase: N/A
Study type: Interventional

Perioperative fasting is an essential patient safety measure to reduce the risk of pulmonary aspiration of gastric contents, a rare but potentially catastrophic complication of anesthetic and airway management. Anesthesiologists' concern about aspiration and the increasing awareness towards the negative impact of prolonged restriction of oral intake have shaped the current fasting guidelines. However, due to the perceived safety of prolonged fasting and practical considerations, adoption of the fasting guidelines is suboptimal. Gastric ultrasound is a quick, non-invasive method to evaluate gastric contents and aspiration risk. Gastric ultrasound can accurately discriminate between solid particles and fluid content, and mathematical models can reliably predict the volume of the gastric contents from the gastric antral area (GAA). This project aims to use gastric ultrasound to provide new data that can support management strategies in perioperative patients, that ensure both a low aspiration risk and an adequate nutritional support. The investigators will test the hypothesis that commercially available liquid meals can be safely used preoperatively. A pilot crossover, study on healthy volunteers will be conducted to determine the gastric emptying time of high-calorie drinks, as compared to clear fluid.

NCT ID: NCT04972357 Completed - Bariatric Surgery Clinical Trials

Bariatric Procedures and Changes Gastric Passage

BIP
Start date: October 1, 2018
Phase:
Study type: Observational

Gastric emptying measured with scintigraphy in patients after standard Roux-en-Y Gastric Bypass (S-RYGB), Banded-RYGB (B-RYGB) or Extended pouch-RYGB (E-RYGB).

NCT ID: NCT04571866 Completed - Gastric Emptying Clinical Trials

Gastric Emptying After Bread Consumption

Start date: October 20, 2020
Phase: N/A
Study type: Interventional

The rate of gastric emptying is proposed to be one of the major determinants of postprandial glycemia. A slower gastric emptying will thus result in a less pronounced rise in blood glucose, which is especially desirable in diabetes care as it will highly influence the overall glycemic control. The present study aims to investigate the rate of gastric emptying and postprandial blood glucose levels in response to the intake of bread with different dietary fiber-content. Though bread is one of the major sources of dietary carbohydrates in Central- and Northern Europe, the mechanism and the metabolic effects of bread consumption, however, is investigated in a limited number of studies.

NCT ID: NCT04263415 Completed - PCOS Clinical Trials

The Effects of Semaglutide on Taste, Tongue Tissue Transcriptome, Gastric Emptying and Central Neural Response in Women With PCOS and Obesity

Start date: November 2, 2019
Phase: Phase 4
Study type: Interventional

The purpose of the study is to explore the effects of GLP-1 receptor agonist (GLP-1 RA) semaglutide on modulation of taste sensitivity, tongue tissue transcriptome, modulation of neural response in central reward processing regions and gastric emptying rate. In addition, we aim to investigate the associations between semaglutide induced modulation of taste sensitivity, neural responses and gastric emptying with changes in body mass, eating- behavioural pattern, food perception and food intake.

NCT ID: NCT04228497 Completed - Gastric Emptying Clinical Trials

Ultrasound Assessment of Gastric Residual Volume in Children Scheduled for Elective Surgery After Clear Fluids Fasting for One Versus Two Hours: a Comparative Study

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Ultrasound guided comparison of gastric residual volume after clear fluid fasting for one versus two hours in pediatrics scheduled for elective surgery.

NCT ID: NCT04092049 Completed - Gastric Emptying Clinical Trials

Lollipop on Gastric Emptying

Start date: October 21, 2019
Phase: N/A
Study type: Interventional

To investigate the effect of chewing lollipop on gastric volume and gastric emptying in healthy volunteers drinking water.

NCT ID: NCT03694509 Completed - Gastric Emptying Clinical Trials

Gastric Emptying After Tea With Milk in Pregnancy.

Start date: October 30, 2018
Phase: N/A
Study type: Interventional

The aim of the study is to assess the difference in gastric emptying using ultrasound of pregnant patients following a cup of tea with milk or a similar volume of water.

NCT ID: NCT03410147 Completed - Healthy Clinical Trials

A Dose-finding and Feasibility Study for a Prolonged 13C-octanoate Breath Test for Gastric Emptying

ANTERO-AC-7
Start date: February 9, 2018
Phase: N/A
Study type: Interventional

The objective of this dose-finding and feasibility study is to establish the optimal 13C-octanoate concentration to be used with slowly infused enteral nutrition to perform a prolonged gastric emptying test using the breath test. More specifically, the aim is to discover the 13C-octanoate concentration that induces a steady state hourly 13C-recovery. This would allow to implement the prolonged breath test protocol in a future clinical investigation in critically ill patients.