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Dyspepsia clinical trials

View clinical trials related to Dyspepsia.

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NCT ID: NCT02365701 Completed - Dyspepsia Clinical Trials

Study of Motilitone to Treat Functional Dyspepsia

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

This study is to evaluate efficacy of the investigational drug Motilitone at 90 mg in patients with Functional Dyspepsia as measured by change in maximum tolerated volume and aggregate symptom score on the nutrient drink test.

NCT ID: NCT02360696 Completed - Dyspepsia Clinical Trials

Functional Dyspepsia (FD) - Clinical Response to Montelukast in Children

Start date: August 2014
Phase:
Study type: Observational

Duodenal eosinophilia has been associated with dyspepsia in adults and the investigators have previously described the finding of duodenal mucosal eosinophilia in 71-79% of children undergoing diagnostic endoscopy. Previous studies in children have shown positive response to montelukast with approximately 50% finding complete relief and 20-30 percent showing no response. There are a number of factors that have the potential to contribute to the observed variability in response to montelukast. These include variability in: 1. systemic drug exposure (drug absorption, biotransformation and/or elimination) 2. regulation of leukotriene biosynthesis 3. cysteinyl leukotriene receptors and downstream mediators 4. patient disease phenotype (e.g. Functional Gastrointestinal Disorder (FGID) disease classification, psychologic profile) In this study, the investigators propose to utilize biopsy specimens stratified by drug response to identify candidate gene expression modules that will be validated in a prospective study design. The overall goal of this program is to develop a signature of montelukast response that can be applied not only to eosinophilic gastroenteritis, but more generally to other diseases, such as asthma, where the drug is widely used with variable success.

NCT ID: NCT02358486 Recruiting - Dyspepsia Clinical Trials

The Effect and Mechanism of Acupuncture on Functional Dyspepsia

Start date: January 2015
Phase: N/A
Study type: Interventional

The aim of the study is to investigate the effect of acupuncture on functional dyspepsia compared with sham control. The study aims to clarify the mechanism of acupuncture by assessing functional magnetic resonance imaging and metabolomics.

NCT ID: NCT02340312 Completed - Clinical trials for Functional Dyspepsia

Functional Dyspepsia Microbiome Study

Start date: January 2015
Phase:
Study type: Observational

Recurrent abdominal pain has long been acknowledged to be the most common chronic pain entities in children. The purpose of this study is to describe the microbiome in children with FD and to explore relationships between the microbiome and postprandial distress syndrome, anxiety scores, and mucosal biomarkers or anxiety. The specific goals of this study are to: 1) Determine the frequencies and relative proportions for specific bacteria or bacteria phyla in children with FD in both duodenal mucosal specimens and stool samples. 2) Determine if the frequencies or proportions of specific bacteria or bacteria phyla differ between children with and without PDS. 3) Determine bi-variate correlations between bacteria/phyla frequency, bacteria/phyla proportions, anxiety scores, and mucosal biomarkers, respectively.

NCT ID: NCT02320981 Completed - Clinical trials for Functional Dyspepsia

Mucosal Impedance in Pediatric Population

Start date: August 2014
Phase: N/A
Study type: Observational

Our hypothesis is that patients with GERD and/or Eosinophilic Esophagitis (EE) have lower esophageal impedance measurements when compared to patients who do not have GERD or EE.

NCT ID: NCT02306941 Completed - Abdominal Pain Clinical Trials

Internet-delivered CBT for Functional Abdominal Pain in Adolescents - a Pilot

Start date: March 2015
Phase: N/A
Study type: Interventional

This pilot-study aims to evaluate the treatment effects and feasibility of an internet-delivered CBT-program adjusted for adolescents with functional abdominal pain and functional dyspepsia.

NCT ID: NCT02296021 Completed - Dyspepsia Clinical Trials

Helicobacter Pylori Eradication With Berberine Quadruple Therapy Versus Bismuth-containing Quadruple Therapy

Start date: November 2014
Phase: Phase 4
Study type: Interventional

This study aims at evaluating efficacy and safety of berberine-containing quadruple therapy(berberine, esomeprazole, clarithromycin and amoxicillin) versus bismuth-containing quadruple therapy (bismuth,esomeprazole,clarithromycin and amoxicillin) in H. pylori eradication. It is hypothesized that berberine-containing quadruple therapy is non-inferior to bismuth-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: NCT02282995 Recruiting - Dyspepsia Clinical Trials

Effect of Genetic Association With Functional Dyspepsia and Mood Disorders

FDFDR
Start date: August 2012
Phase: N/A
Study type: Observational

Background: Functional dyspepsia (FD) is one of the commonest digestive disorders. The pathophysiology of functional dyspepsia is uncertain. Risk factors include genetics, gender, age, helicobacter pylori infection, etc. However, few reported the association of genetic contribution to the development of FD and mood disorder. Indication: Functional dyspepsia patients Study center(s): Prince of Wales Hospital, Hong Kong Aims: - To evaluate genetic factors on development of functional dyspepsia & common mood disorders - To evaluate genetic factors on the severity of function dyspepsia & mood disorders - To develop a diagnostic test for classification of functional dyspepsia by plasma ghrelin and serotonin expression - To collect sleep data for future use - To save blood sample for future retrospective diagnostic or genetic examination Study design: Case-control cross sectional study Number of subjects: Total of 1200 subjects (300 FD patients + 300 relatives of FD patients FDR) and (300 Controls + 300 FDR) Patient population: Functional dyspepsia patients age 18-60 Duration of study: 1 May 2012 - 30 April 2013 Primary variable(s): Genetic polymorphisms of targeted genes, plasma ghrelin and serotonin expression Secondary variable(s): FD global symptom assessment and symptom scores Number of visits: 1 Hypotheses: - Shared genetic factors contribute to the development of FD and common psychological disorders - FD patients contribute to suppression of plasma ghrelin and serotonin expression compared to healthy controls

NCT ID: NCT02277431 Completed - Abdominal Pain Clinical Trials

Probiotic Supplementation Among Adults With Recurrent Gastrointestinal Symptoms

Start date: December 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Participants experiencing recurrent gastrointestinal symptoms in this double-blind, randomized, controlled trial will receive either a commercially-available probiotic dietary supplement or placebo. The investigators hypothesize that participants in the probiotic dietary supplement group will experience greater improvement in their gastrointestinal symptoms than participants in the placebo group.

NCT ID: NCT02197143 Completed - Dyspepsia Clinical Trials

A Comparison of Efficacy of Intravenous Esomeprazole and Ranitidine Treatment of Dyspeptic Pain

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

- Currently, Proton Pump Inhibitors and H2Receptor Blockers are widely used by emergency physicians in Turkey for the treatment of patients with dyspepsia. - The objective of the study was to assess whether intravenous esomeprazol has superior dyspeptic pain reduction compared with ranitidine or hydrotalcid in emergency department (ED) adults - The investigators second aim was to compare recurrent dyspeptic pain within 24 hours after discharge and cost of treatments in the treatment of dyspepsia.