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Dyspepsia clinical trials

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NCT ID: NCT02633930 Completed - Dyspepsia Clinical Trials

Helicobacter Pylori Eradication With Berberine Quadruple Therapy Versus Clarithromycin Quadruple Therapy

Start date: December 2015
Phase: Phase 4
Study type: Interventional

This study aims at evaluating efficacy and safety of berberine-containing quadruple therapy(berberine, lansoprazole, bismuth and amoxicillin) versus clarithromycin-containing quadruple therapy (clarithromycin,lansoprazole, bismuth and amoxicillin) in H. pylori eradication. It is hypothesized that berberine-containing quadruple therapy is non-inferior to clarithromycin-containing quadruple therapy. Patients with confirmed H. pylori positive status will be randomized to one of the treatments described above. At week 2 and 6 follow-up visits, a urea breath test(UBT) will be performed to confirm eradication.

NCT ID: NCT02621359 Recruiting - Dyspepsia Clinical Trials

A Two Week Nitazoxanidebased Quadruple Regimen

Start date: January 2015
Phase: Phase 3
Study type: Interventional

Helicobacter pylori (H. pylori) infection is a global health problem as it is associated with peptic ulcers, chronic gastritis, duodenitis, and stomach cancer. Therefore, the eradication of the pathogen is of critical importance to reduce H. pylori-related complications . However, due to increasing antibiotic resistance, eradication of Helicobacter pylori has become more challenging. With a great decline in the eradication rate of standard triple therapy for Helicobacter pylori to below 70% in many countries. Treatment with triple therapy, which is the most frequently recommended, fails to eradicate H. pylori in approximately 20% of cases .

NCT ID: NCT02620696 Completed - Dyspepsia Clinical Trials

Effect of Netazepide on Omeprazole-induced Changes in Chromogranin A and Gastrin

Start date: November 2009
Phase: Phase 1
Study type: Interventional

Hypergastrinaemia induced by proton pump inhibitor (PPI) treatment is reported to cause ECL-cell and parietal-cell hyperplasia, and rebound hyperacidity and dyspepsia after PPI withdrawal. The objective of the study was to determine the dosage regimen of netazepide, a gastrin/CCK2 receptor antagonist, required to inhibit the trophic effects of PPI-induced hypergastrinaemia. Six groups of 8 healthy subjects participated in a randomised, double-blind, placebo-controlled exploratory study of esomeprazole 40 mg daily for 28 days, and netazepide 1, 5 or 25 mg, or placebo daily during the last 14 days of esomeprazole dosing, or 14 days after esomeprazole withdrawal. Serum gastrin and plasma chromogranin A (CgA) were measured regularly from study start until at least 1 week after the last dose. Dyspepsia was monitored after esomeprazole withdrawal.

NCT ID: NCT02618070 Completed - Clinical trials for Functional Dyspepsia

Cognitive Modulation of Dyspeptic Symptom During Food Ingestion in Functional Dyspepsia Patients Cognitive Modulation

Start date: March 2016
Phase: N/A
Study type: Interventional

In this functional magnetic resonance imaging study, effects of different information of fat content of high or low fat will be examined in FD patients and healthy volunteers (n=30, respectively). These data will provide a better understanding of symptom generation following food ingestion in general as well as in patients with respective functional gastrointestinal disorders.

NCT ID: NCT02611414 Recruiting - Dyspepsia Clinical Trials

Effectiveness of tDCS for the Treatment of Functional Dyspepsia

Start date: January 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Functional dyspepsia is a very common disorder of great challenge to clinical management. A therapeutic targets is up-regulation of visceral pain threshold. The transcranial direct current stimulation (tDCS) is a novel therapy that pursues these properties, besides its safety and easy adherence. There is a great need of new treatments for functional dyspepsia. There is no current study evaluating tDCS for this disease.

NCT ID: NCT02604576 Completed - Dyspepsia Clinical Trials

Efficacy of Bromopride and Simethicone Versus Bromopride in Functional Dyspepsia

Start date: January 17, 2017
Phase: Phase 3
Study type: Interventional

Multi-center, randomized, superiority, double blind clinical trial to asses the efficacy of fixed-dose combination of bromopride and simethicone versus isolated bromopride on research participants diagnosed with functional dyspepsia.

NCT ID: NCT02592239 Completed - Dyspepsia Clinical Trials

Hedonic Perception and Brain Activity Response to Meal

Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the relationship between brain activity and the perception of subjective hedonic sensations in response to a meal using functional MRI.

NCT ID: NCT02570776 Recruiting - Dyspepsia Clinical Trials

UBT as a Diagnostic Tool for HP Prevalance

Start date: December 2013
Phase: N/A
Study type: Observational

The prevalence of H. pylori infection in Pakistan is unknown and investigators want to assess it in dyspeptic patients utilizing UBT. At the same time investigators want to validate UBT sensitivity and specificity in Pakistani patients

NCT ID: NCT02567578 Terminated - Clinical trials for Functional Dyspepsia

A Trial to Evaluate the Efficacy and Safety of YH12852 in Patients With Functional Dyspepsia

Start date: October 2015
Phase: Phase 2
Study type: Interventional

This is a multicenter, randomized, double-blind, placebo-controlled dose-finding phase 2 trial to evaluate the efficacy and safety of YH12852 in patients with functional dyspepsia.

NCT ID: NCT02566876 Completed - Clinical trials for Irritable Bowel Syndrome

Bifidobacteria In Children With Abdominal Pain-Associated Functional Gastrointestinal Disorders

Start date: December 2013
Phase: Phase 4
Study type: Interventional

Abdominal pain (AP)-associated functional gastrointestinal disorders (FGIDs), particularly Irritable Bowel Syndrome (IBS) and Functional Dyspepsia (FD), are common in pediatrics, and no safe and effective treatment is available. Although probiotics have shown promising results in adults, few studies have been published in children. The Bifidobacterium Infantis, Bifidobacterium Breve and Bifidobacterium Longum are the most important beneficial bacteria in children and represent 95% of the total bacterial population in the intestine of breastfed infant. Objectives: 1) To evaluate the effect of oral administration of a mixture of Bifidobacteria on the improvement of frequency and intensity of AP in children with FD and IBS. 2) To evaluate the effect of oral administration of a mixture of Bifidobacteria on quality of life in children with FD and IBS.