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Gastroesophageal Reflux Disease clinical trials

View clinical trials related to Gastroesophageal Reflux Disease.

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NCT ID: NCT01058070 Completed - Clinical trials for Gastroesophageal Reflux Disease

An Observational Clinical Feasibility Study of the Magnetic Esophageal Sphincter

Start date: February 2007
Phase: N/A
Study type: Interventional

Magnetic Esophageal Sphincter implant is intended to reinforce Esophageal Sphincter function in the treatment of Gastroesophageal Reflux Disease (GERD)

NCT ID: NCT01057992 Completed - Clinical trials for Gastroesophageal Reflux Disease

A Prospective Evaluation of the Torax Medical Inc. Magnetic Esophageal Sphincter

Start date: March 2007
Phase: Phase 1/Phase 2
Study type: Interventional

A medical device to augment weak lower esophageal sphincter function.

NCT ID: NCT01053585 Completed - Clinical trials for Gastroesophageal Reflux Disease

Structure and Function of the Gastro-esophageal Junction

Start date: February 2007
Phase: N/A
Study type: Interventional

Aims of research project: To identify key features of the gastro-esophageal junction (structure and function) that protects the esophagus from gastro-esophageal reflux investigated by combined high resolution manometry and magnetic resonance imaging. Hypothesis: 1. Functional factors including GEJ function (e.g. sphincter pressure) and proximal gastric distension determine whether or not TLESR occurs; however 2. Structural factors including separation of GEJ anatomy, intra-gastric distribution of the meal and secretions determine whether TLESR is accompanied by no reflux event, gas reflux (belching) or reflux of ingested food and gastric secretion ('true reflux'). 3. Initial findings by descriptive studies in healthy volunteers (study #1) and patients with mild to moderate gastro-esophageal reflux disease (study #2) will be further interrogated by a randomized, double-blind control trial of baclofen in patients with GORD; a medication that inhibits reflux by effects on GOJ function (study #3) .

NCT ID: NCT01043185 Completed - Clinical trials for Gastroesophageal Reflux Disease

A Study to Estimate Effect of 4 Different Doses of AZD3355 on Reflux Episodes, Which Patients With Gastroesophageal Reflux Disease (GERD) May Experience

Start date: December 2009
Phase: Phase 2
Study type: Interventional

The purpose of the study is to estimate what effect 4 different doses of AZD3355 will have on the number of reflux episodes, in patients who have GERD and still experience symptoms despite proton pump inhibitor (PPI) treatment.

NCT ID: NCT01041105 Completed - Clinical trials for Gastroesophageal Reflux Disease

Gastric Bypass After Previous Anti-reflux Surgery

RYGBafterARS
Start date: December 2008
Phase: N/A
Study type: Observational

The goal of this study is to describe the clinical presentation, indications, and operative treatment as well as assess the morbidity, mortality, and overall performance of revisional Roux-en-Y gastric bypass (RYGB) after either failed or functional antireflux surgery "ARS" in obese patients. With such information, we hope to determine which features might assist us in advancing our knowledge about Gastro-Esophageal Reflux Disease "GERD", the best option for primary ARS, and mechanisms of failure in the obese population as well as in identifying predictors of outcome after revisional surgery in this population.

NCT ID: NCT01039558 Completed - Clinical trials for Gastroesophageal Reflux Disease

The Effect of Lansoprazole in Combination With Ecabet Sodium for Gastroesophageal Reflux Disease

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

We will estimate the responses of lansoprazole and ecabet sodium combination therapy and compare with lansoprazole and placebo therapy in patients who need additional therapy after standard proton pump inhibitor treatment for 4week or more in recurrent gastroesophageal reflux disease.

NCT ID: NCT01027975 Completed - Clinical trials for Gastroesophageal Reflux Disease

Comparison of Laparoscopic Nissen Versus Thal Fundoplication in Children

Start date: July 1998
Phase: N/A
Study type: Interventional

Laparoscopic fundoplication is increasingly performed in paediatric surgery. Many types of fundoplication are performed, each has advantages and disadvantages. The Nissen operation is the most frequently performed procedure in the U.K., however it can be associated with post-operative dysphagia. The relative benefits between Nissen and other fundoplication techniques in children are still uncertain. The aim of our study was to compare the long-term outcomes following laparoscopic Nissen fundoplication with laparoscopic Thal fundoplication in children.

NCT ID: NCT01026103 Completed - Hypertension Clinical Trials

Tri Staple Technology Stapler Used in Gastric Bypass

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

The objectives of this clinical trial are to assess in a pilot setting the overall performance and safety of the Endo GIA™ Stapler with Endo GIA™ SULU with Tri-Staple™ Technology when used in a gastric bypass procedure.

NCT ID: NCT01020890 Completed - Clinical trials for Gastroesophageal Reflux Disease

Prevalence of Gastroesophageal Reflux Disease in Primary Care Patients With Upper Gastrointestinal Symptoms

Start date: November 2009
Phase: N/A
Study type: Observational

The purpose of this study is to provide data on the gastroesophageal reflux disease (GERD) prevalence as percentage of patients with upper gastrointestinal (GI) symptoms that are identified with GERD using the Gerd-Q Questionnaire.

NCT ID: NCT01005251 Completed - Clinical trials for Gastroesophageal Reflux Disease

Investigate the Effect of Different Doses of Lesogaberan (AZD3355) as add-on to PPI in GERD Patients With Partial Response to PPI

Start date: October 2009
Phase: Phase 2
Study type: Interventional

This study is being carried out to see whether AZD3355 is an effective treatment as an add-on to PPI therapy in patients with Gastroesophageal Reflux Disease (GERD) with a partial response to PPI and to compare this with Proton Pump Inhibitor (PPI) treatment alone. Another goal of the study is to examine which of the investigated doses of AZD3355 is optimal for treatment of these patients. This study will also measure levels of drug in the blood and see how well it is tolerated.