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Digestive System Diseases clinical trials

View clinical trials related to Digestive System Diseases.

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NCT ID: NCT01405612 Completed - Clinical trials for Digestive System Disorders

Study to Examine the Effect of Ulimorelin on the Pharmacokinetics of Midazolam in Healthy Volunteers

Start date: June 2011
Phase: Phase 1
Study type: Interventional

An open-label, single centre, randomised, cross-over study to examine the effect of ulimorelin on the pharmacokinetics of midazolam after repeat dose administration of ulimorelin in healthy volunteers.

NCT ID: NCT01405599 Completed - Clinical trials for Digestive System Disorders

Evaluation of the Pharmacokinetics of Ulimorelin in Subjects With Hepatic Impairment and Healthy Subjects

Start date: June 2011
Phase: Phase 1
Study type: Interventional

Evaluation of the effect of hepatic impairment on the pharmacokinetics of ulimorelin after a single intravenous (IV) dose in order to identify potential patients at risks in terms of severity of hepatic dysfunction and to determine whether their dosage should be adjusted.

NCT ID: NCT01397747 Completed - Colorectal Cancer Clinical Trials

Multi-Target Colorectal Cancer Screening Test for the Detection of Colorectal Advanced Adenomatous Polyps and Cancer

DeeP-C
Start date: June 2011
Phase: N/A
Study type: Observational

The primary objective is to determine the sensitivity and specificity of the Exact Colorectal Cancer (CRC) screening test for colorectal cancer, using colonoscopy as the reference method. Lesions will be confirmed as malignant by histopathologic examination. The secondary objective is to compare the performance of the Exact CRC screening test to a commercially available FIT assay, both with respect to cancer and advanced adenoma. Lesions will be confirmed as malignant or precancerous by colonoscopy and histopathologic examination.

NCT ID: NCT01382563 Completed - Clinical trials for Eosinophilic Esophagitis

Registry for Eosinophilic Gastrointestinal Disorders (REGID)

EoE
Start date: November 2012
Phase:
Study type: Observational

Develop Registry tool

NCT ID: NCT01373918 Completed - Cholestasis Clinical Trials

Low Dose Fat for the Prevention of Liver Disease in Babies With Gastrointestinal Disorders

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

Neonates with congenital/acquired gastrointestinal disorders are at high risk for Parenteral Nutrition Associated Cholestasis (PNAC). Besides enteral nutrition, standard therapies to prevent and treat PNAC have been limited and marginal. Recently, the dose and composition of standard intravenous fat emulsions have implicated in the development and progression of PNAC. In this study, neonates with congenital/acquired gastrointestinal disorders will be randomized, in a unblinded fashion, to receive either the standard dose of an intravenous omega-6 fatty acid emulsion or a low dose of an intravenous omega-6 fatty acid emulsion throughout their course of PN or until hospital discharge, death or 100 days of life, whichever comes first. The primary outcome will be the presence of cholestasis.

NCT ID: NCT01360502 Completed - Anemia Clinical Trials

Safety of Capsule Endoscopy in Patients With Implantable Cardiac Devices

Start date: December 2009
Phase: N/A
Study type: Observational

This is a prospective study designed to assess safety and potential influence of the MiroCam on cardiac pacemaker and implantable cardiac defibrillator.

NCT ID: NCT01304394 Completed - Clinical trials for Infant, Premature, Diseases

Safety During Use of Paediatric Triple Chamber Bag Formulas

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

The primary objective of this study was to provide daily information on the performance safety of the Ped3CB in practical therapeutic use in pediatric patients.

NCT ID: NCT01273077 Completed - Clinical trials for Gastrointestinal Diseases

Evaluation of Universal Rotavirus Vaccination Program

Start date: December 2010
Phase:
Study type: Observational

Two rotavirus vaccines have been authorized for use in Canada: RotaTeq®, Merck Frost Canada, Inc. and Rotarix®, Glaxo Smith Kline (GSK). In contrast to the United States, Australia and several other western countries, neither rotavirus vaccine is offered in a publicly funded program in Canada. A universal rotavirus immunization program offered to all children has the potential to prevent moderate to severe forms of the disease associated with rotavirus, with associated decreased disease burden and health care costs. This demonstration project seeks to evaluate the effect of the implementation of a universal infant immunization program with Rotarix employing two different program delivery models (public health delivery or physician office delivery) in comparison to a jurisdiction where routine immunization is not provided. Only evaluation of the program will be the subject of this study.

NCT ID: NCT01262755 Completed - Clinical trials for Gastroesophageal Reflux Disease

Temple Registry for the Investigation of African American Gastrointestinal Disease Epidemiology

TRIAGE
Start date: April 2010
Phase: N/A
Study type: Observational

DESCRIPTION: Minimal data exists on the prevalence of gastroesophageal reflux disease in minority populations. Specific objectives of this K24 research project are to: (1) Provide an estimate of the prevalence of gastroesophageal reflux disease in an urban, African American population; (2) Determine whether specific risk factors including diet, tobacco use, physical activity, and psychosocial stress are important in the targeted population. We will also measure height, weight, and waist/hip circumference to determine the impact of central obesity on reflux. PUBLIC HEALTH RELEVANCE: This research will help doctors to understand the frequency and risks for esophageal reflux disease (heartburn) in African Americans.

NCT ID: NCT01260168 Completed - Colorectal Cancer Clinical Trials

Multi-marker Stool Test for Detection of Colorectal Neoplasia: Marker Panel Selection and Technical Development Studies

Start date: October 2010
Phase: N/A
Study type: Observational

The objective of this study is to confirm the sensitivity of a stool DNA test for detection of colorectal cancer and pre-cancer. Another objective is to provide anonymous, clinically characterized specimens for a bio-repository for future colorectal cancer-related test development.