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Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated Children

A Double-blind Randomized Controlled Clinical Trial Investigating the Use of Intravenous Dextrose for Dehydration and Ketosis in Children With Gastroenteritis and Dehydration.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01343758
Enrollment
188
Registered
2011-04-28
Start date
2007-01-31
Completion date
2011-07-31
Last updated
2012-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dehydration, Gastroenteritis

Brief summary

Infants and young children often become infected with gastroenteritis leading to vomiting and diarrhea. This can lead to dehydration, one of the most common complaints in the Pediatric Emergency Department. These children are often in need of treatment with intravenous (IV) fluids. While the investigators know that IV fluids work, it is not clear which type or how much fluid is the best amount to give. Currently, the most common type of IV fluid given is salt water, also called normal saline. In contrast to adults, infants and young children with dehydration often have a build up of a certain type of acid in their blood which can perpetuate the nausea, vomiting, and general malaise associated with gastroenteritis. The investigators feel that giving these children IV fluids with lots of sugar (in addition to the salt) reduces the acid more rapidly than giving just salt water alone. In a prior study, the investigators have shown that children who receive lower amounts of sugar in the IV fluids return to the Emergency Department more often for a second visit. Based on this study, the investigators believe that children who receive the sugar-salt solution will do better than children who receive just normal saline. The investigators will determine if the sugar-salt solution is better by giving equal numbers of children the sugar-salt solution and normal saline and then see what happens to each child. The investigators will monitor who needs to be admitted, how much each child vomits, how much each child drinks, and also the level of acid in the blood before and after getting the IV fluid. After the study is completed, the investigators can compare the two different groups (children who received the sugar-salt solution versus children who received normal saline alone) to determine if one group had greater improvement and better clinical outcome than the other.

Interventions

OTHER5% dextrose in normal saline

Subjects will be randomized to receive a intravenous fluid bolus of 5% dextrose in normal saline or normal saline

Sponsors

Abbott
CollaboratorINDUSTRY
Boston Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
6 Months to 6 Years
Healthy volunteers
Yes

Inclusion criteria

* 6 months to 6 years of age * Gastroenteritis * Requires IV fluids for dehydration

Exclusion criteria

* Chronic disease * Comorbid condition * Received IV fluids or antiemetics in the last 12 hours * Symptoms for more than 7 days * Blood glucose less than 40

Design outcomes

Primary

MeasureTime frameDescription
Admission RateDuring emergency department visitThe investigators will measure what percentage of patients in each treatment group are admitted.

Secondary

MeasureTime frameDescription
Change in Serum Ketones1 and 2 hours after treatment givenThe investigators will measure the change in serum ketones at 1 and 2 hours after the study fluid is given and compare the mean change in each treatment group.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026