Trial Of Normal Saline Versus Ringer's Lactate In Paediatric Trauma Patients

PHASE4CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

May 31, 2013

Primary Completion Date

August 31, 2014

Study Completion Date

December 31, 2014

Conditions
Trauma
Interventions
DRUG

Normal Saline

Patients randomized to Normal Saline arm, will receive intravenous normal saline for all resuscitation and maintenance fluid for a period of 24 hours commencing on presentation to hospital.

DRUG

Ringer's Lactate

Patients randomized to Ringer's Lactate arm, will receive intravenous Ringer's Lactate for all resuscitation and maintenance fluid for a period of 24 hours commencing on presentation to hospital.

Trial Locations (1)

N6A5W9

Children's Hospital, London Health Sciences Centre, London

All Listed Sponsors
lead

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

NCT01692769 - Trial Of Normal Saline Versus Ringer's Lactate In Paediatric Trauma Patients | Biotech Hunter | Biotech Hunter