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Clinical trialNCT04201704RecruitingInterventional

Effect of Giving Reduced Fluid in Children After Trauma

SponsorColumbia UniversityEnrollment250Critical IllnessFluid TherapyGeneral SurgeryPediatricsWounds and Injuries
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This study is designed to help decide how much intravenous (IV) fluid should be given to pediatric trauma patients. No standard currently exists for managing fluids in critically ill pediatric trauma patients, and many fluid strategies are now in practice. For decades, trauma patients got high volumes of IV fluid. Recent studies in adults show that patients actually do better by giving less fluid. The investigators do not know if this is true in children and this study is designed to answer that question and provide guidelines for IV fluid management in children after trauma.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • John R. Oishei Children'S Hospital of Buffalo

    Buffalo, New York, United States

    Not, yet, recruiting
  • Columbia University Irving Medical Center Newyork-Presbyterian Morgan Stanley Children'S Hospital

    New York, New York, United States

    Recruiting
  • University of Rochester, Golisano Children'S Hospital

    Rochester, New York, United States

    Recruiting
  • Le Bonheur Children'S Hospital

    Memphis, Tennessee, United States

    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
27 Aug 2018
Primary completion
31 Aug 2027
Completion
30 Sept 2027
Last update posted
7 May 2026
Registered enrollment
250
Registry id
NCT04201704

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 11 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.