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Gastroparesis clinical trials

View clinical trials related to Gastroparesis.

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NCT ID: NCT01378884 Withdrawn - Gastroparesis Clinical Trials

The Use of Domperidone for Gastroparesis

Start date: March 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether domperidone can be used safely and effectively for patient with gastroparesis.

NCT ID: NCT01326117 Withdrawn - Nausea Clinical Trials

Daily Tadalafil and Gastric Emptying Time in Diabetic Gastroparesis

Start date: April 2011
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that in adult patients with diabetic gastroparesis with Type 1 diabetes (HbA1c ≤ 10.5%), daily tadalafil use will significantly improve gastric emptying compared to baseline as measured by gastric emptying time.

NCT ID: NCT00944593 Withdrawn - Clinical trials for Diabetic Gastroparesis

Gastric vs Jejunal Feeding in Diabetic Gastroparesis

Start date: n/a
Phase: Phase 4
Study type: Interventional

Diabetic 'Gastroparesis' or 'Gastroenteropathy' is a condition in which patients suffer episodes of nausea, vomiting, abdominal bloating and pain after eating. These symptoms occur in the absence of any structural abnormality of the stomach, rather abnormal gastric function underlies the condition. Up to one in five patients with type I diabetes experience symptoms consistent with this diagnosis. The effects on diabetic control, physical health and emotional quality of life are severe. Patients do not respond reliably to general supportive management or conventional medications. Surgical options have disappointing results. The need for more effective treatment is acknowledged universally. Feeding into the small bowel beyond the stomach (jejunal feeding) is established management in diabetic patients with gastroenteropathy that are malnourished due to poor oral intake. The benefits have been assumed secondary to improved nutrition and diabetic control; however this assertion has never been studied. Recently we observed that patients with severe gastroenteropathy recovered promptly and could eat normally during and for a few hours after jejunal feeding. These observations suggest that jejunal feeding has 'quasi-pharmacological' effects in patients with gastroenteropathy. One attractive explanation for these observations is that gastroenteropathy represents a failure of oral intake to 'switch' the stomach from the fasted to the fed state. According to this hypothesis, jejunal feeding 'restores' the normal fed state by bypassing the dysfunctional stomach. This project will assess the effects of feeding on gastrointestinal (GI) sensory and motor function in diabetic gastroenteropathy. Healthy volunteers and diabetic controls without symptoms will also be investigated. Studies will assess: 1. Effects on GI symptoms and function to gastric distension in fasted and fed states 2. Effects on GI symptoms and function to oral vs. nasogastric delivery of a test meal 3. A trial of gastric feeding with and without prior jejunal feeding on GI symptoms and function Non-invasive magnetic resonance imaging (MRI) techniques will be applied to assess complex gastric response to feeding. In addition the effects of feeding on symptoms and gastric function will be related to alterations in GI hormones and autonomic nervous activity (eg cardiovagal tone) to assess how the integrated response of the GI tract to feeding fails in patients with diabetic gastroenteropathy. The primary aim of this project is to assess the effectiveness of jejunal feeding in the management of diabetic gastroenteropathy. However, by defining the processes that 'switch' gastric function between the fasted and the fed states and control gastric emptying, we hope also to identify candidate targets for more effective pharmacologic treatment of this severe disease. - Trial with medical device

NCT ID: NCT00622804 Withdrawn - Stomach Cancer Clinical Trials

Comparison Study for Bile Reflux and Gastric Stasis in Patients After Distal Gastrectomy

Start date: July 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the degree of bile reflux and gastric stasis according the reconstruction methods after distal subtotal gastrectomy for gastric cancer, and to find out the proper method. We collect ninety patients who undergo distal gastrectomy for gastric cancers for this study from 5 institutions and randomly divide into 3 groups according to reconstruction methods: 1) Billroth-II (B-II), 2) Roux en Y gastrojejunostomy (RY-GJ) and 3) uncut Roux en Y gastrojejunostomy (uncut RY-GJ).

NCT ID: NCT00568373 Withdrawn - Gastroparesis Clinical Trials

Gastric Pacemaker Implantation for Gastroparesis

HUD
Start date: June 2007
Phase: N/A
Study type: Interventional

Gastric pacemakers and/or temporary gastric stimulators will be implanted in eligible patients.