Clinical Trials Logo

Gastroparesis clinical trials

View clinical trials related to Gastroparesis.

Filter by:

NCT ID: NCT00776360 Completed - Clinical trials for Postprocedural Delayed Gastric Emptying

The Effect of Oxytocin on the Gastric Emptying

Start date: December 2008
Phase: Phase 0
Study type: Interventional

The investigators are going to examine whether oxytocin has a prokinetic effect on gastric emptying in patients suffering from gastro paresis. Oxytocin infusion will be compared with sodium chloride infusion.

NCT ID: NCT00765895 Completed - Clinical trials for Idiopathic Gastroparesis

Nortriptyline for Idiopathic Gastroparesis

NORIG
Start date: January 2009
Phase: Phase 3
Study type: Interventional

The principal objective of this multicenter, randomized, placebo-controlled trial is to evaluate whether treatment with nortriptyline will improve gastroparesis symptoms compared with placebo.

NCT ID: NCT00733551 Completed - Gastroparesis Clinical Trials

Evaluation of the Safety, Tolerability and Pharmacokinetics of Repeat Oral Doses of GSK962040 Administered to Healthy Adult Subjects.

Start date: September 23, 2008
Phase: Phase 1
Study type: Interventional

This study will evaluate the safety, tolerability and exposure of repeat escalating oral doses of GSK962040.

NCT ID: NCT00682877 Completed - Gastroparesis Clinical Trials

A Comparison of SmartPill Capsule With Scintigraphy for Determining Gastric Residence Time - Over 65 Years Old

GETOver65
Start date: July 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine the correlation between gastric residence time of the SmartPill Capsule and the time required for partial emptying of a standard radiolabeled meal as measured by gastric emptying scintigraphy for subjects 65 years of age and older.

NCT ID: NCT00639808 Completed - Diabetes Mellitus Clinical Trials

Safety and Efficacy of IV Infusion of Investigational Agent (TZP-101) in Patients With Diabetic Gastroparesis

Start date: August 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether TZP-101 is safe in people with diabetes. Also to determine if TZP-101 is effective in increasing the gastric emptying rate in diabetic patients.

NCT ID: NCT00612014 Completed - Diabetes Mellitus Clinical Trials

Safety and Efficacy of IV Infusion of Investigational Agent (TZP-101) in Patients With Severe Diabetic Gastroparesis

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

The purpose of this study is to determine whether TZP-101 is effective in the treatment of symptomatic gastroparesis due to diabetes.

NCT ID: NCT00595621 Completed - Gastric Stasis Clinical Trials

Multi-Channel Gastric Electrical Stimulation for the Treatment of Gastroparesis

Start date: February 2006
Phase: N/A
Study type: Interventional

Investigate the safety and efficacy of multi-channel gastric electrical stimulation in the treatment of patients with severe diabetic gastroparesis refractory to standard therapy.

NCT ID: NCT00562848 Completed - Gastroparesis Clinical Trials

A Study to Evaluate Safety, Side Effects, Muscle Activity and Speed of Gastric Emptying of GSK962040

Start date: September 10, 2007
Phase: Phase 1
Study type: Interventional

Motilin is a peptide whose action is controlled by motilin receptors located in the gut. Action of Motilin at motilin receptors increases the gastric emptying rate (rate of emptying of food and fluid from the stomach). Compounds which stimulate motilin receptors therefore provide a potential approach to the treatment of a range of clinical conditions where delayed gastric emptying may contribute to symptoms, such as enteral feeding intolerance (post-operative or intensive care patients), gastroparesis, diabetic gastroparesis, and functional dyspepsia. This study is the First Time In Human study for the motilin receptor agonist, GSK962040.

NCT ID: NCT00501657 Completed - Diabetes Mellitus Clinical Trials

Effects of Sitagliptin on Gastric Emptying in Healthy Subjects

Start date: July 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effects of the drug, sitagliptin, on the rate at which the stomach empties, and the release of gut hormones and blood glucose concentrations, after a mashed potato meal in healthy subjects. Sitagliptin has been shown to reduce the blood glucose (sugar) response to a meal and this may potentially be due to slowing of stomach emptying. This is particularly relevant to people who have diabetes, in whom normalization of elevated blood glucose levels is important to maintain health.

NCT ID: NCT00492622 Completed - Clinical trials for Gastroesophageal Reflux Disease

Pharmacokinetics of Immediate-Release vs. Delayed-Release Omeprazole in Gastroparesis

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the blood drug levels of two prescribed medications, immediate-release omeprazole 40 mg powder and delayed-release omeprazole 40 mg capsule to determine which drug is better absorbed in patients with a slow stomach emptying (gastroparesis). Delayed-release omeprazole has a protective coating to prevent the drug omeprazole from being neutralized by stomach acid. Immediate-release omeprazole has sodium bicarbonate (antacid) which neutralizes the stomach acid, eliminating the need for a protective coating. Immediate-release omeprazole suspension may have a more rapid pharmacokinetic profile and greater overall drug absorption in gastroparesis.