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Gastroenteritis clinical trials

View clinical trials related to Gastroenteritis.

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NCT ID: NCT03125473 Completed - Clinical trials for Norovirus Gastroenteritis

Dose-Optimization Trial of VXA-G1.1-NN in Healthy Volunteers

Start date: April 7, 2017
Phase: Phase 1
Study type: Interventional

A Phase 1b, randomized, double-blind, dose-ranging trial to determine the safety of different dosing regimens an adenoviral-vector based norovirus vaccine (VXA-G1.1-NN) expressing GI.1 VP1 and dsRNA adjuvant administered orally to healthy volunteers

NCT ID: NCT03052361 Terminated - Gastroenteritis Clinical Trials

Triage Administration of Ondansetron for Gastroenteritis in Children

Start date: July 15, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators aim to assess whether ondansetron given at triage can reduce the number of patients requiring emergency department observation in children with acute gastroenteritis. The investigators will also assess the improvement of patient comfort and total length of stay

NCT ID: NCT03046342 Recruiting - Gastroenteritis Clinical Trials

Gastroenteritis in Pediatric Population of Qatar

GE
Start date: March 10, 2015
Phase:
Study type: Observational

Comparison of clinical and laboratory diagnosis for cause of Gastroenteritis(GE) depending on the clinical manifestation.Identifying the sources of viral, bacterial and parasitic GE in Pediatric population of Qatar

NCT ID: NCT03021109 Completed - Dehydration Clinical Trials

Assessment of Volume Status by Bedside Ultrasound in Children With Acute Gastroenteritis

Start date: December 2016
Phase: N/A
Study type: Interventional

The purpose of the study is assessment of volume status by bedside ultrasound in children with acute gastroenteritis

NCT ID: NCT03000296 Active, not recruiting - Crohn's Disease Clinical Trials

Autologous Unselected Hematopoietic Stem Cell Transplantation for Refractory Crohn's Disease

AutoChron
Start date: October 2013
Phase: N/A
Study type: Interventional

This study evaluates the safety and clinical benefits of a therapeutic approach using the cyclophosphamide (Cy) + thymoglobulin® (ATG) + granulocyte colony-stimulating factor (G-CSF) conditioning regimen followed by autologous hematopoietic stem cell transplantation (HSCT) rescue in the treatment of refractory Crohn's disease. Adverse events, and clinical and endoscopic conditions will be assessed at different short and long-term time points.

NCT ID: NCT02989350 Completed - Clinical trials for Acute Gastroenteritis

Efficacy of Lactobacillus Reuteri DSM 17938 for the Treatment of Acute Gastroenteritis in Children

Start date: January 16, 2017
Phase: N/A
Study type: Interventional

Acute gastroenteritis (AGE) is one of the most common diseases among children. Oral rehydration therapy is the key treatment. According to the 2014 guidelines developed by the ESPGHAN probiotics may be considered in the management of children with AGE in addition to rehydration therapy. Considering that evidence on L reuteri remains limited, the investigators aim to assess the efficacy of L reuteri DSM 17938 for the treatment of AGE in children. Children vaccinated and not vaccinated against rotavirus will be evaluated separately. Two independent reports (rotavirus-vaccinated and non-vaccinated children) are planned.

NCT ID: NCT02941107 Active, not recruiting - Clinical trials for Viral Gastroenteritis Due to Rotavirus

Optimising Rotavirus Vaccine in Aboriginal Children

ORVAC
Start date: March 27, 2018
Phase: Phase 4
Study type: Interventional

Australian Indigenous children, particularly those living in remote communities, suffer a disproportionately high burden of rotavirus gastroenteritis disease. Despite the introduction of rotavirus vaccine into the Northern Territory (NT) Immunisation Schedule in 2006, the rate of hospitalization for rotavirus in NT Aboriginal children < 5 years continues to be high, and the rate ratio of rotavirus hospitalisations for Indigenous versus non-Indigenous children has actually increased. The reasons for sub-optimal vaccine response are not completely understood, but both reduced vaccine immune responses and low vaccine coverage are likely to be important factors. The purpose of this study is to determine if Aboriginal children who receive an additional dose of RV1 between the ages of 6 and 12 months, will have an increase anti-rotavirus serum IgA seroconversion and decreased medical presentations with gastroenteritis in the first three years of life, compared to those who receive placebo.

NCT ID: NCT02902445 Completed - Gastroenteritis Clinical Trials

Glycan Attachment Specificity, Toward ROtavirus Vaccine IMprovement GASTROVIMc (Clinical Investigation)

Gastrovimc
Start date: February 28, 2017
Phase:
Study type: Observational

The GASTROVIM research explores the links between individual genetic susceptibility, genetic variability of rotavirus strains and effectiveness of immunization with the rotavirus vaccination: a clinical investigation to assess glycan attachment specificity, toward rotavirus vaccine improvement.

NCT ID: NCT02900703 Recruiting - Gastroenteritis Clinical Trials

Surveillance of Rotavirus Gastroenteritis

Rotavirus
Start date: February 2007
Phase: N/A
Study type: Observational

- Epidemiological studies have shown the diversity of resistance genotypes and the evolution of their prevalence in the paediatric population. This large study conducted in a context of very low vaccination coverage will generate more precise data on the natural epidemiological evolution of rotavirus, notably the G9 genotype, which has appeared relatively recently. - This study will allow us to identify and document rare or unusual strains of human or animal origin. The complete genetic characterization of these strains will also make it possible to study their ability to recombine and to assess the risk of emergence. Among these still rare strains, the investigators are particularly monitoring G12 rotavirus, whose ability to recombine raises the risk of emergence. - For at least one of the centres taking part in the study, the paediatric population studied will be given strong vaccination coverage. It will be extremely interesting to compare the results obtained in the vaccinated population with non-vaccinated children to assess the impact of this vaccination on the distribution of rotavirus genotypes

NCT ID: NCT02897271 Completed - Clinical trials for Eosinophilic Esophagitis

Characteristics of Eosinophilic Gastritis, Enteritis, and Colitis in a Multi-Site Cohort

Start date: August 2016
Phase:
Study type: Observational

The purpose of this study is to investigate features of patients with Eosinophilic Gastrointestinal Disorders (EGIDs) other than Eosinophilic Esophagitis (EoE) alone, including Eosinophilic Gastritis (EG), Eosinophilic Gastroenteritis (EGE), and Eosinophilic Colitis (EC).