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Dyspepsia clinical trials

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NCT ID: NCT00786214 Completed - Clinical trials for Functional Dyspepsia

Treatment of Functional Dyspepsia With Acupuncture

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

Functional dyspepsia (FD) is one of the most common chronic gastrointestinal disorders affecting humans. Existing therapies for FD are still far from satisfactory and new therapies are constantly being sought. Acupuncture has been used for the alleviation of functional gastrointestinal symptoms in several non-controlled studies. This study aims to investigate the therapeutic efficacy of acupuncture in patients with FD.

NCT ID: NCT00772837 Completed - Clinical trials for Helicobacter Pylori Infection

Effect of Eradication of Helicobacter Pylori on the Dyspeptic Symptoms

EEHPDS
Start date: August 2006
Phase: N/A
Study type: Interventional

Helicobacter pylori eradication and its impact on symptoms in patients with non-ulcer dyspepsia remain controversial . Many studies have examined the effect of H. pylori eradication on dyspeptic symptoms, but the results have been conflicting and inconclusive, with as many studies yielding positive as negative results. Some studies have shown a significant (although weak) symptomatic improvement after H. pylori eradication, and while other yielding negative results. A recent Cochrane review has comprehensively demonstrated that H.pylori eradication therapy has a small but statistically significant effect in H.pylori positive non-ulcer dyspepsia. An economic model suggests this modest benefit may still be cost effective . However it is difficult to reconcile these results in areas with very high prevalence of H. pylori infection such as Pakistan since no such studies have been conducted in developing countries. The investigators hypothesize that eradication of Helicobacter pylori (H. pylori) leads to a sustained improvement in symptoms of patients diagnosed with H. pylori associated functional (non-ulcer) dyspepsia.

NCT ID: NCT00764374 Completed - Dyspepsia Clinical Trials

A Long-term, Open-label, Uncontrolled Trial of YM443 (Z-338) in Patients With Functional Dyspepsia

Start date: August 2008
Phase: Phase 3
Study type: Interventional

To examine the safety and efficacy of Z-338 (YM443) after long-term administration in patients with functional dyspepsia, and also to examine the pattern of long-term administration.

NCT ID: NCT00761358 Completed - Clinical trials for Functional Dyspepsia

To Verify the Efficacy of Z-338 in Subjects With Functional Dyspepsia

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to verify the superior efficacy of Z-338 to placebo in subjects with Functional Dyspepsia, focusing on the assessment of subjective symptoms.

NCT ID: NCT00761254 Terminated - Nausea Clinical Trials

Domperidone for Relief of Gastrointestinal Disorders

Start date: August 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to make Domperidone available to patients with gastrointestinal disorders who have failed standard therapy and who might benefit from it.

NCT ID: NCT00723502 Completed - Dyspepsia Clinical Trials

Efficacy and Safety Study of Finafloxacin Used in Helicobacter Pylori Infected Patients

FLASH
Start date: September 2008
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to compare the H. pylori eradication rates with Finafloxacin in combination with Amoxicillin or Esomeprazole. The secondary objective is to evaluate and compare the safety and tolerability of multiple oral doses of Finafloxacin plus Amoxicillin versus Finafloxacin plus Esomeprazole.

NCT ID: NCT00693407 Completed - Clinical trials for Functional Dyspepsia

Study of Endogenous Inhibitory Modulation During Gastric and Somatic Stimulation

Start date: September 2008
Phase: N/A
Study type: Interventional

Visceral hypersensitivity as evidence of central sensory sensitization is evident in many patients with functional disorders such as functional dyspepsia (FD) and irritable bowel syndrome (IBS). We recently demonstrated both somatic hypersensitivity and abnormal endogenous pain modulation in IBS, both of which indicate central sensitization as a crucial mechanism in IBS. Endogenous pain mechanisms regulate, fine-tune and integrate sensory and homeostatic, including neuroendocrine, immune, motor and autonomic nervous system processes. Hitherto, no studies have investigated the role endogenous pain modulation in FD. Abnormal modulation could explain several of the symptom complexes associated with FD and provide a rationale for exploration of new treatments. The current study was designed to 1. investigate the gastric sensitivity in FD patients and healthy controls during gastric capsaicin stimulation 2. assess the endogenous pain inhibitory modulation system in FD patients and healthy controls during heterotopic stimulation

NCT ID: NCT00673972 Withdrawn - Clinical trials for Functional Dyspepsia

Comparative Study of Epigastric Pain Syndrome and Postprandial Distress Syndrome

Start date: April 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare postprandial distress syndrome and epigastric pain syndrome in demographics psychological features, infection of Helicobacter pylori, gastric emptying and therapeutic response to lansoprazole.

NCT ID: NCT00673699 Not yet recruiting - Dyspepsia Clinical Trials

The Role of Narrow-Band Imaging Endoscopy in Diagnosing Gastric Intestinal Metaplasia

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

The purpose of this study is to determine if endoscope with NBI(narrow banding imaging)can detect intestinal metaplasia( consider pre malignant condition) and use a targeting biopsy in case of suspected intestinal metaplasia

NCT ID: NCT00663897 Completed - Clinical trials for Functional Dyspepsia

Lansoprazole Versus Mosapride for Functional Dyspepsia

Start date: May 2008
Phase: Phase 4
Study type: Interventional

Functional dyspepsia is a common symptom complex with significant impact on quality of life. There is no standard treatment for functional dyspepsia but therapeutic efficacy of proton pump inhibitor (PPI) and prokinetic agent have been proved in subsets of patients. This study has two aims: - first is to compare the therapeutic efficacy of lansoprazole (a PPI) and mosapride (a prokinetic agent) for functional dyspepsia - second is to investigate whether different subgroups of functional dyspepsia (e.g., epigastric pain syndrome and postprandial distress syndrome) respond differently to PPI and prokinetic agent.