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Peptic Ulcer clinical trials

View clinical trials related to Peptic Ulcer.

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NCT ID: NCT03320538 Recruiting - Clinical trials for Peptic Ulcer Disease

Efficacy and Safety of Hou Gu Mi Xi in Patients With Peptic Ulcer Diseases

Start date: July 10, 2017
Phase: N/A
Study type: Interventional

This trial aims to determine whether Jiangzhong Hou Gu® Mi Xi™ is an effective intervention to improve symptoms and indicators in patients with spleen qi deficiency and peptic ulcer diseases.

NCT ID: NCT02436018 Recruiting - Gastric Cancer Clinical Trials

WEI NASAL JET for The Sedation of Outpatient Upper Gastrointestinal Endoscopy

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

Low pulse oximetry is the most common adverse events during sedation for upper gastrointestinal endoscopy. The main reason is the glossoptosis after sedation. In present study a new designed nasopharyngeal airway embedded with jet ventilation catheter(WEI NASAL JET) will be utilized in order to reduce the hypoxia. At the same time the safety will be evaluated.

NCT ID: NCT02434978 Recruiting - Clinical trials for Peptic Ulcer Bleeding

Doppler-guided Endoscopic Treatment in Peptic Ulcer Bleeding

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

The present study is a randomized controlled trial (RCT) that examines if the outcome of peptic ulcer bleeding could be improved by use of doppler-guided endoscopic treatment.

NCT ID: NCT01979549 Recruiting - Gastric Cancer Clinical Trials

Adverse Events During Upper Gastrointestinal Endoscopy

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

The primary objective is to investigate the adverse events during upper gastrointestinal endoscopy with and without sedation in Chinese population

NCT ID: NCT01845168 Recruiting - Clinical trials for Bleeding Peptic Ulcer

Prevention of Gastric Ulcer Bleeding by Using "Computer-alert" in General Practice

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate if a computerised decision-support tool used in general practice, can reduce the frequency of peptic ulcer bleeding related to the use of NSAIDs (Non-Steroidal-antiinflammatory-drug) and ASA( Acetylsalicylic acid) . On the basis of "The Danish general medical database" it is possible to develope a computerised decision-support tool, which enables the general practitioner (GP) in a "pop-up" window to get information on each patients risk-factors, when prescribing NSAID and aspirin to a patient at risk. This will give the general practitioner the oppurtunity to choose a different type of preparation or prescribe ulcer-preventive medicine at the same time. The decision-support tool will be tested in a randomized trial among general practitioners. The aim is to reduce the occurence of peptic ulcer bleeding. The expected outcome is a reduction in half of the total numbers of peptic ulcers.

NCT ID: NCT01182597 Recruiting - Peptic Ulcers Clinical Trials

Oral Versus IV Proton Pump Inhibitor in High-risk Bleeding Peptic Ulcers After Endoscopic Hemostasis

Start date: August 2010
Phase: Phase 3
Study type: Interventional

Endoscopic hemostasis has been documented by a number of clinical studies to be effective in decreasing rebleeding, need for emergency surgery, and hospitalization days. Studies showed adjuvant treatment with proton pump inhibitor (PPI) after initial endoscopic hemostasis reduced recurrent ulcer bleeding. However, the optimal dose and route of adjuvant PPI therapy remains controversial. A recent study demonstrated frequent oral PPI offered similar acid control as currently recommended intravenous infusion PPI did in patients with bleeding ulcers. The investigators hypothesize that an frequent oral PPI treatment has similar benefit as proton pump inhibitor infusion in patient with bleeding ulcers after combined endoscopic hemostasis.

NCT ID: NCT00854776 Recruiting - Peptic Ulcer Clinical Trials

Peptic Ulcer Disease in Ischemic Heart Patients Taking Aspirin and Clopidogrel With or Without Proton Pump Inhibitor

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

Studies showed that combined use of clopidogrel and aspirin had a 25 % reduction of risk on myocardial infarction and stroke in patients who undergone percutaneous coronary intervention (PCI) when compared with use of aspirin alone. However, major GI bleeding rose in combined group than aspirin group. Use of proton pump inhibitor (PPI) which diminishes gastric acid secretion effectively reduces aspirin or clopidogrel associated ulcer or/and ulcer bleeding in general population and high risk patients. The investigator hypothesis is whether use of PPI can reduce ulcer and ulcer complication in patients taking both clopidogrel and aspirin.

NCT ID: NCT00709046 Recruiting - Bleeding Clinical Trials

High Dose Versus Standard Dose Proton Pump Inhibitor (PPI) in High-risk Bleeding Peptic Ulcers After Combined Endoscopic Treatment

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

The study was designed to evaluate the efficacy an adjuvant use of standard dose or high dose of proton pump inhibitor after combined endoscopic hemostasis therapy.

NCT ID: NCT00687336 Recruiting - Clinical trials for Peptic Ulcer Hemorrhage

Helicobacter Pylori Empiric Treatment in Ulcer Bleeding

HETUB
Start date: March 2008
Phase: Phase 4
Study type: Interventional

The goal of the study is to compare the effectiveness of empirical Helicobacter pylori treatment compared with treatment depending on diagnostic tests for Helicobacter pylori in patients with Upper gastrointestinal bleeding due to peptic ulcer. Main hypothesis is that empirical treatment will reduce the number of patients lost to follow-up thus improving the cure rates of Hp infection.

NCT ID: NCT00471029 Recruiting - Peptic Ulcer Clinical Trials

Compare Efficacy of Gastric Acid Suppression by Oral and Intravenous Administration of Esomeprazole in Patients With Peptic Ulcer

NPH
Start date: September 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the gastric acid suppression profile among different regimen (Oral Vs Intravenous)of administration of proton pump inhibitor - Esomeprazole by 24hours intragastric pH monitoring.