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Acute Gastroenteritis clinical trials

View clinical trials related to Acute Gastroenteritis.

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NCT ID: NCT06090708 Completed - Clinical trials for Acute Gastroenteritis

Yogurt Probiotic Bacteria on Relieving Young Children Acute Gastroenteritis

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to test the effect of mothers' application of yogurt probiotic bacteria on relieving their young children's acute gastroenteritis in children had two to five years old. The main hypothesis is children with acute gastroenteritis who receive yogurt probiotic bacteria exhibit less diarrhea, vomiting and dehydration than those who don't.The study subjects were divided into two equal groups (probiotic study group and control group).

NCT ID: NCT05076461 Completed - Clinical trials for Acute Gastroenteritis

Ondansetron Versus Domperidone for Treating Vomiting in Acute Gastroenteritis in Children

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

Most of the trials conducted comparing ondansetron and domperidone have been conducted among children aged below 5 or 6 years of age while no study from Pakistan has compared efficacy of these antiemetic agents among children up to 12 years of age. The findings of present study will give valuable evidence about the effectiveness of these antiemetic agents to prevent vomiting among children suffering with acute gastroenteritis at a resource limited setting of South Punjab, Pakistan.

NCT ID: NCT04682860 Completed - Abdominal Pain Clinical Trials

Management of Abdominal Pain in Acute Gastroenteritis Patients With Hyoscine Butylbromide

Start date: September 8, 2021
Phase: Phase 4
Study type: Interventional

One of the most common complaints of admission to the emergency room is gastroenteritis. One of the most common complaints in acute gastroenteritis is abdominal pain. The aim of our study is to investigate whether hyoscine butylbromide used within the indication has an effect on abdominal pain due to acute gastroenteritis. The main purpose of our study is to reduce the pain of the patient at 30th and 60th minutes compared to 0th minute.

NCT ID: NCT04555200 Completed - Dehydration Clinical Trials

Continuous Enteral Rehydration by Nasogastric Tube With ORS in Children With Acute Gastroenteritis

GEA
Start date: June 1, 2018
Phase:
Study type: Observational

When oral rehydration is impossible, enteral rehydration via the nasogastric route has been the recommended method of rehydration since 2008 by ESPGHAN ( European Society for Paediatric Gastroenterology Hepatology and Nutrition ), for children with acute gastroenteritis. However, these recommendations are rarely followed in France. These recommendations were not applied in the Children's Emergency Department of BREST University Hospital. The investigators changed the protocol and shared it with the caregivers of the emergency unit. The investigators studied the impact of this change of protocol

NCT ID: NCT04463355 Completed - Clinical trials for Acute Gastroenteritis

Video Discharge Instructions for Pediatric Gastroenteritis in an Emergency Department

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

Video discharge instructions (VDI) have been suggested as a useful strategy to improve discharge instructions in pediatric emergency units. The goal of this study is to evaluate if the addition of VDI to usual verbal information improved the comprehension of information provided to caregivers of patients who consult for acute gastroenteritis (AGE). An open-label, parallel, randomized trial was designed, enrolling patients who consult for AGE. First, caregivers answer a written test concerning AGE characteristics and management. They are randomly allocated to a control group, which receives verbal discharge instructions, or to an intervention group, which additionally receives video discharge instructions. After discharge, caregivers are contacted by telephone and answer the same test. Main outcome measure is difference between test scores in the first and the second tests, secondary endpoints are how many caregivers score 5/5 on the second test, as well as rate of return visits and caregivers satisfaction with the information received.

NCT ID: NCT03539913 Completed - Clinical trials for Acute Gastroenteritis

Efficacy and Safety of Probiotics in the Treatment of Acute Gastroenteritis in Children

SABINA
Start date: June 19, 2017
Phase: Phase 4
Study type: Interventional

- Primary Objective: o To assess the efficacy of the probiotics in reducing the duration of diarrhea in children suffering from acute gastroenteritis. - Secondary Objectives: - To assess the efficacy of the probiotics in improving the frequency and consistency of stools. - To assess the efficacy of the probiotics in avoiding recurrence of diarrhea. - To assess the efficacy of the probiotics on the disease severity. - To assess the safety and tolerability of the studied probiotics.

NCT ID: NCT03234777 Completed - Pediatric ALL Clinical Trials

Evaluating a Knowledge Translation Tool for Parents

Start date: November 30, 2017
Phase: N/A
Study type: Interventional

Diarrhea and vomiting in children is a common reason to visit the emergency department. There has been a lot of research on how best to treat children with diarrhea and vomiting who visit the emergency department; however, the care children receive varies by healthcare provider and across hospitals. Additionally, there are things parents can do at home to help manage childhood diarrhea and vomiting and potentially avoid a trip to the emergency department. This shows an urgent need for knowledge translation, that is, efforts to align research knowledge and healthcare practice. Actively involving parents in healthcare decisions has the potential to bridge this gap; however, there is little research on the best ways to communicate complex health information to parents of sick kids. In 2013, a national needs assessment was conducted with parents seeking care for their kids in general emergency departments (trekk.ca). This survey showed that 39% of parents looked for information about their child's health prior to coming to the emergency department and that 44% of these parents looked for this information on the internet. This means that the development and evaluation of digital tools to give parents timely and effective child health information has the potential to reduce unnecessary emergency department visits, empower parents in health decision-making, and ultimately improve child health outcomes. In this project, parents will be actively involved in the evaluation of a digital tool, a whiteboard animation video, designed to communicate the best research evidence on the treatment and management of vomiting and diarrhea in children. In this pilot trial, parents in two emergency departments will be randomized to view the video or a sham video, and then provide quantitative and qualitative data on the potential effectiveness of the video, the perceived benefit and value of the knowledge translation intervention for pediatric vomiting and diarrhea, the feasibility of using iPads and an electronic data collection platform to conduct research with this population, the time required to complete data collection, and parents' willingness to participate in future, similar research.

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: 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: 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.