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Gastroesophageal Reflux clinical trials

View clinical trials related to Gastroesophageal Reflux.

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NCT ID: NCT00911534 Completed - Clinical trials for Symptomatic Gastroesophageal Reflux Disease (sGERD)

Comparing the Efficacy, Safety, and Tolerability of Rabeprazole ER 50 mg With Placebo in Subjects With Symptomatic Gastroesophageal Reflux Disease (sGERD)

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

The purpose of this study is to compare the efficacy, safety and tolerability of rabeprazole extended release (ER) 50 mg with placebo in subjects with symptomatic gastroesophageal reflux disease (sGERD).

NCT ID: NCT00901004 Completed - Clinical trials for Gastroesophageal Reflux Disease

The Clinical Significance of Minimal Change in Reflux Esophagitis Based on the Gastroesophageal Reflux Disease Questionnaire

MIGHT
Start date: April 2009
Phase: N/A
Study type: Observational

The purpose of this study is to define the endoscopic findings of minimal change that is significant to clinical significant reflux esophagitis. Through this, the investigators want to estimate the applicability of minimal change findings of reflux esophagitis to the clinic.

NCT ID: NCT00890201 Completed - Clinical trials for Pancreaticobiliary Reflux

Pancreaticobiliary Reflux in Patients Without Cholelithiasis

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

Pancreaticobiliary reflux has been found in patients with cholelithiasis and gallbladder cancer associated with normal pancreaticobiliary union. However, the presence of pancreaticobiliary reflux has not been studied in patients without gallstones (healthy gallbladders). The authors believe that pancreaticobiliary reflux might be a normal phenomenon in patients with and without gallstones, although in patients with cholelithiasis it might constitute a pathological condition associated with dismotility of the biliary tree and the sphincter of Oddi.

NCT ID: NCT00886197 Completed - Clinical trials for Gastroesophageal Reflux Disease

Diagnostic Efficacy of Narrow Band Imaging in Patients With Gastroesophageal Reflux Disease

Start date: September 2007
Phase: N/A
Study type: Observational

Gastroesophageal reflux disease (GERD) is a common disorder in Asia that includes erosive and non-erosive counterparts. The evaluation of intra-esophageal damage is of paramount importance because patients with erosive and those with non-erosive GERD have distinct manifestations and prognoses. Although proton-pump inhibitor (PPI) is the treatment of choice for erosive patients with excellent therapeutic response, the majority of reflux patients can be classified with non-erosive reflux disease (NERD).Narrow-band imaging (NBI) is a novel, noninvasive optical technique that adjusts reflected light to improve the contrast of capillary patterns compared with conventional illumination. Based on the standard procedure of sequential conventional white-light, NBI, and magnified NBI, the investigators have validated the reliability of the diagnostic testing. The investigators will also enroll NERD patients to test their therapeutic response to rabeprazole. The investigators can find out the best strategy to identify the PPI responder.

NCT ID: NCT00885469 Completed - Clinical trials for Gastroesophageal Reflux Disease

PillCam® ESO 2 in Esophageal Pathologies

MA-76
Start date: December 2007
Phase:
Study type: Observational

Study Hypothesis: - PillCamâ„¢ ESO-2 will demonstrate equivalent accuracy parameters as compared to blinded esophagogastroduodenoscopy (EGD) in detecting suspected Barrett's esophagus, detecting and grading esophagitis. - PillCamâ„¢ ESO will demonstrate all safety parameters as compared to EGD - PillCamâ„¢ ESO-2 will demonstrate better patient's satisfaction as compared to EGD

NCT ID: NCT00884247 Completed - GERD Clinical Trials

Structured Treatment of Gastroesophageal Reflux in a Company Health Care Setting, -Effect on Quality of Life, Symptoms and Productivity

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

The study aims to evaluate if a GERD treatment programme, in accordance with current regional recommendations, in a company health care setting, has an impact on health related quality of life (HRQoL), symptoms, and productivity in GERD patients.

NCT ID: NCT00872755 Completed - Dysphagia Clinical Trials

Nissen and Gastroplasty in Gastroesophageal Reflux Disease (GERD)

Start date: January 2002
Phase: Phase 4
Study type: Interventional

Laparoscopic Nissen Fundoplication has established itself as the procedure of choice in the surgical management of the majority of patients suffering from gastroesophageal reflux disease (GERD). Postoperative paraesophageal herniation has incidence ranges up to 7% in the immediate postoperative period. This randomized controlled study was scheduled to investigate the role of the posterior gastropexy, in combination with laparoscopic Nissen fundoplication, in prevention of paraesophageal herniation and improvement of postoperative results, in surgical treatment of GERD.

NCT ID: NCT00868296 Completed - Clinical trials for Gastroesophageal Reflux

Open Label Safety Study of Enteric-Coated Spheroid Suspension in Infants Aged Less Than 12 Months With Presumed Gastroesophageal Reflux Disease (GERD)

Start date: March 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to provide additional information on safety and tolerability after multiple does of pantoprazole. Only patients who successfully completed the 3001B3-331 study (NCT00362609) or 3001B3-333 study (NCT00259012) are eligible to participate in this study.

NCT ID: NCT00865995 Completed - Clinical trials for Gastroesophageal Reflux

Pepsin As A Biomarker For Aspiration

Start date: February 2008
Phase: N/A
Study type: Observational

Evaluation of tracheal pepsin as a biomarker for aspiration

NCT ID: NCT00864396 Completed - Clinical trials for Laryngopharyngeal Reflux

Twice Daily Prevacid for the Treatment of Laryngopharyngeal Reflux

Start date: July 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether treatment with twice-daily Lansoprazole 30mg (Prevacid 30mg) and behavioral modifications for reflux is superior to treatment with behavioral modifications for reflux alone in the treatment of laryngopharyngeal reflux (LPR).