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Peptic Ulcer clinical trials

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NCT ID: NCT02165488 Completed - Liver Fibrosis Clinical Trials

Frequent Ketamine Use and Gastrointestinal, Liver and Biliary Sequelae

Start date: June 2014
Phase:
Study type: Observational

30% of ketamine users complain of abdominal discomfort. Long-term ketamine use is associated with hepatotoxicity and pathologic changes to the biliary tract. Yet the prevalence of gastrointestinal and hepatobiliary pathologies in ketamine users has not been well-described. The investigators plan to recruit a large number of ketamine users based on referrals from different Psychiatry clusters in Hong Kong and to investigate the underlying cause of abdominal discomfort, describe the prevalence of different gastrointestinal and hepatobiliary pathologies and describe their long-term outcome.

NCT ID: NCT02152904 Completed - Clinical trials for Peptic Ulcer Bleeding

Risk Factors of Rebleeding After Peptic Ulcer Bleeding: a Nationwide Cohort Study

KPUB
Start date: April 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of the investigators study is to investigate the factors associated with rebleeding in patients with peptic ulcer bleeding.

NCT ID: NCT02088385 Completed - Clinical trials for Bleeding Peptic Ulcers

Hemospray Versus the Combined Conventional Technique for Endoscopic Hemostasis of Bleeding Peptic Ulcers : A Pilot Study

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

Hemospray (TC-325, Cook Medical Inc, Winston-Salem, NC, USA), a new adsorptive nanopowder hemostatic agent for endoscopic treatment of high-risk bleeding peptic ulcers, provides significant ease of administration compared to the combined conventional technique of saline-adrenaline injection with mechanical clip or heater probe applications. The Hemospray powder is easily applied on ulcers at difficult endoscopic positions and ulcers with fibrotic bases, where the combined conventional technique has limited efficacy. Building up on preliminary work from small single-arm studies, the investigators aim to establish the efficacy and safety of Hemospray in treating bleeding peptic ulcers in comparison with the combined conventional technique. The investigators propose a pilot study to establish our centre's feasibility of performing a prospective, randomized, parallel group trial, which compares the efficacy of Hemospray with the combined conventional technique, in the endoscopic treatment of high-risk bleeding peptic ulcers. Patients with high-risk bleeding peptic ulcers will be treated with Hemospray to determine its initial hemostasis rate (defined as endoscopically verified cessation of bleeding for at least 5 minutes after endoscopic treatment), rebleeding rate (recurrent hemorrhage during a 4-week period following the initial hemostasis) and its safety profile.

NCT ID: NCT02084420 Completed - Peptic Ulcer Clinical Trials

Efficacy/Safety Study as H. Pylori Eradication of Triple Therapy for 7 Days Treatment

Start date: December 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate of efficacy and safety as H.pylori eradiation effect between Ilaprazole and Pantoprazole triple therapy for 7 days treatment in Gastric and/or Duodenal ulcer patients with H.pylori positive infection.

NCT ID: NCT02020603 Completed - Clinical trials for Active Peptic Ulcer Disease/GI Bleeding

Efficacy of Hemostasis by Soft Coagulation Using Endoscopic Hemostatic Forceps for Acute Peptic Ulcer Bleeding

Start date: January 2012
Phase: N/A
Study type: Interventional

Endoscopic high-frequency soft coagulation is available for the management of bleeding or nonbleeding visible vessels during endoscopic submucosal dissection. However, its efficacy on peptic ulcer bleeding has not been elucidated so far. The aim of this study was to evaluate the efficacy of hemostasis with soft coagulation using hemostatic forceps by comparing it with argon plasma coagulation (APC) in a prospective, randomized trial.

NCT ID: NCT01944878 Completed - Cirrhosis Clinical Trials

The Association With Peptic Ulcer Disease and Hepatic Vein Pressure Gradient

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

The aim of this study is to assess the role of portal hypertension of peptic ulcer disease in liver cirrhosis and chronic hepatitis.

NCT ID: NCT01888588 Completed - Clinical trials for Peptic Ulcer [Iowa Type (107680.0010)]

Risk of Uncomplicated Peptic Ulcer in the General Population

Start date: September 2012
Phase: N/A
Study type: Observational

The analyses are conducted in a previous population-based cohort study using The Health Improvement Network database in the UK (Cai et al 2009).The aims of the post hoc analyses are: To estimate the relative risk of uncomplicated symptomatic peptic ulcer (UPU) associated with use of low dose aspirin (ASA) and other anti-inflammatory drugs (NSAIDs, steroids) in the general population To estimate the dose-response and duration-response associated with use of these drugs To estimate the relative risk of UPU associated with naive/non-naive use of low dose ASA in the general population To evaluate the effect of proton pump inhibitors (PPI) (alone or in combination with anti-inflammatory drugs) on the occurrence of UPU in the general population To investigate the management of low dose ASA/oral antiplatelets after UPU

NCT ID: NCT01838109 Completed - Pancreatic Cancer Clinical Trials

Postoperative Oral Nutritional Supplementation After Major Gastrointestinal Surgery

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

Patients who underwent major gastrointestinal surgery is potentially at risk of malnutrition due to reduced oral intake, increased nutritional need, reduced gastrointestinal absorption function, and/or metabolic changes after surgery. The postoperative malnutrition is associated with low quality of life and seems to be related long-term nutritional status. This study is a multicenter, open-labeled prospective randomized clinical trial to examine the effect of postoperative oral nutritional supplements (ONS) after major gastrointestinal surgery by comparing the change of body weight and other nutritional parameters between the experiment group that is supplied with ONS and the control group without ONS.

NCT ID: NCT01828645 Completed - Peptic Ulcer Clinical Trials

Residual Gastric Volume After the Ingestion of a Beverage Containing Carbohydrates Plus Whey Protein

Start date: February 2013
Phase: Phase 2/Phase 3
Study type: Interventional

Carbohydrate enriched-drinks has been used as preoperative treatment up to two hours before anesthesia. These drinks are safe and are not associated to bronchial aspiration during anesthesia. The addition of protein may be beneficial for metabolic preconditioning but there is a few data in literature testing these drinks for safety. The aim of the study will be to investigate the residual gastric volume (RGV) measured during the gastroscopy with abbreviation of fast to 2h with a carbohydrate plus whey protein enriched-drink.

NCT ID: NCT01822600 Completed - Hypoalbuminemia Clinical Trials

The Therapeutic Role of Intravenous Albumin Administration for Peptic Ulcer Bleeding Patients With Hypoalbuminemia

Start date: January 2010
Phase: Phase 4
Study type: Interventional

To test whether intravenous albumin can decrease the rebleeding rate or shorten the duration of hospitalization in patients with peptic ulcer bleeding and hypoalbuminemia.