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Gastroparesis clinical trials

View clinical trials related to Gastroparesis.

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NCT ID: NCT01557296 Completed - Clinical trials for Diabetic Gastroparesis

Evaluation of Diagnostic Methods and Dietary Treatment of Diabetic Gastroparesis

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The objective of the study is in subjects with Insulin Treated Diabetes Mellitus type 1 or 2 and gastroparesis: - validate radiopaque markers with fluoroscopy with gastric scintigraphy method - study the difference of metabolic control including the frequents of hypoglycaemia, gastrointestinal symptoms, quality of life and nutrition state during dietary treatment of food of small particle size compared with food of large particle size - validate the radiopaque markers method and measurement of the blood glucose and gastrointestinal symptoms after a test meal, against the gastric scintigraphy - determine if the function of gastric emptying can be improved after intervention

NCT ID: NCT01519180 Completed - Gastroparesis Clinical Trials

Antro-pyloro-duodenal Motility in Idiopathic Gastroparesis

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

Impaired gastric emptying may cause dyspeptic symptoms including nausea, vomiting and even nutritionnal impairment. Delay in gastric emptying may result from antro-pyloro-duodenal motility impairement.

NCT ID: NCT01481753 Terminated - Clinical trials for Delayed Gastric Emptying

Pancreaticoduodenectomy With or Without Braun Enteroenterostomy: Comparison of Postoperative Pancreatic Fistula and Delayed Gastric Emptying

Start date: December 2009
Phase: N/A
Study type: Interventional

The investigators plan to perform a prospective randomized, head-to-head trial to test the hypothesis that the addition of Braun enteroenterostomy to standard pancreaticoduodenectomy (PD) reconstruction can decrease the rates of Postoperative Pancreatic Fistula (POPF) and/or Delayed Gastric Emptying (DGE).

NCT ID: NCT01469286 Completed - Clinical trials for Diabetic Gastroparesis

Transcutaneous Electroacupuncture for Gastroparesis

TEA
Start date: March 2010
Phase: Phase 1
Study type: Interventional

Gastroparesis is a common disease defined as delayed emptying of the stomach. It is present in at least 20% of about 150 million patients with diabetes worldwide and in more than 20% of patients with functional dyspepsia that affects about 10%-25% of the general population. Gastroparesis is a refractory disease with a lack of therapeutic options. Common symptoms of gastroparesis include nausea, vomiting, early satiety and abdominal bloating. Electroacupuncture (EA) is a combined procedure with acupuncture and electrical current stimulation instead of manual manipulations of the needles. Recent studies in our lab with EA or transcutaneous EA (TEA) have suggested a therapeutic role of EA or TEA for gastric motility disorders. Improvement has been observed with EA or TEA in gastric emptying as well as dyspeptic symptoms. In this project, a micro-stimulator is designed and developed for the TEA therapy. The micro-stimulator is small enough so that it can be attached to the skin next to the stimulation electrodes and therefore the patient can resume normal daily activity while being treated by TEA. This is not only attractive but also more effective since TEA can be performed more often and for longer durations. This exploratory project is designed to study the feasibility, efficacy and certain mechanisms of the proposed method of "wireless" TEA in patients with gastroparesis. Firstly the feasibility of the chronic use the proposed micro-stimulator will be studied. Secondly, the efficacy of the TEA in improving delayed gastric emptying and symptoms of gastroparesis will be investigated in a double-blinded crossover design in patients with diabetic or idiopathic gastroparesis. Thirdly, possible mechanisms involving pathogeneses of gastroparesis with TEA will be investigated.

NCT ID: NCT01467765 Completed - Clinical trials for Postprocedural Delayed Gastric Emptying

The Effect of Elemental Diet on Gastric Emptying

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

In patients with percutaneous endoscopic gastrostomy (PEG) delayed gastric emptying has been speculated as a cause of aspiration pneumonia. Elemental diet may facilitate gastric emptying in PEG patients as compared with regular liquid enteral nutrients, resulting in the prevention of aspiration pneumonia.

NCT ID: NCT01460550 Recruiting - Clinical trials for Postprocedural Delayed Gastric Emptying

A Prospective Randomized Controlled Multicenter Trial of Delayed Gastric Emptying (DGE) After Pancreaticoduodenectomy Evaluating by Gastrointestinal Reconstruction

Start date: November 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the incidence of delayed gastric emptying in patient with pancreaticoduodenectomy between antecolic and retrocolic gastrointestinal reconstruction.

NCT ID: NCT01452815 Completed - Clinical trials for Diabetes Mellitus, Type 2

Affects of Once-daily Oral Administration of TZP-102 on the Treatment of Symptoms Associated With Diabetic Gastroparesis

Start date: September 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test the safety and effectiveness of two dosage levels (10mg and 20mg) of TZP-102 compared to placebo (capsule that looks like the study drug but contains no active drug), administered once-daily for 12 weeks, in diabetic subjects with symptoms associated with gastroparesis.

NCT ID: NCT01394055 Completed - Gastroparesis Clinical Trials

Study to Assess Pharmacodynamics of RM-131 in Patients With Diabetic Gastroparesis

Start date: July 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the pharmacodynamic (PD) and pharmacokinetic (PK) profile and the safety and tolerability of RM-131 in patients with diabetes mellitus and delayed gastric emptying.

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: NCT01329211 Terminated - Gastroparesis Clinical Trials

Needs Assessment Evaluating Quality of Life Issues for Gastroparesis Patients and Caregivers

Start date: January 2010
Phase: N/A
Study type: Observational

The project will involve conducting a Needs Assessment for Gastroparesis patients and their caregivers with the goal of identifying quality of life issues associated with this disease. Identifying these issues will ameliorate management and support systems for gastroparesis currently existent in the community and, hopefully, provide information for the establishment of more resources to assist the patients and their families.