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

NCT ID: NCT04555200

Last Updated: 2020-09-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

88 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-06-01

Study Completion Date

2019-10-02

Brief Summary

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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

Detailed Description

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The main purpose was to assess the proportion of children rehydrated by nasogastric tube(NG) after protocol change. Secondary outcomes were to assess hospital length of stay and sides effects.

It is a retro and prospective study. The first phase took place from June to September 2018 and the second from June to September 2019. Any child presenting to pediatric emergencies for acute gastroenteritis requiring nonoral rehydration was included.

Conditions

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Acute Gastroenteritis Dehydration

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

Any child presenting to pediatric emergencies for acute gastroenteritis requiring nonoral rehydration was included

Exclusion Criteria

* acute gastroenteritis on return from tropical countries
* child with endocrine system diseases requiring parenteral rehydration
* history of chronic pathology requiring enteral feeding
Minimum Eligible Age

1 Day

Maximum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Brest

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Nadege Delaperriere, Doctor

Role: PRINCIPAL_INVESTIGATOR

CHRU Brest

Locations

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CHRU de Brest (urgences pédiatriques)

Brest, , France

Site Status

Countries

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France

Other Identifiers

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29BRC19.0130

Identifier Type: -

Identifier Source: org_study_id

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