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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ANZCTR
Last refreshed on: 12 February 2018
Main ID:  ACTRN12617000047392
Date of registration: 10/01/2017
Prospective Registration: No
Primary sponsor: Urban Flaring
Public title: Sodium concentration as a predictor for perforated appendicitis in children
Scientific title: Sodium concentration as a predictor for perforated appendicitis in children
Date of first enrolment: 6/06/2016
Target sample size: 80
Recruitment status: Completed
URL:  http://www.anzctr.org.au/ACTRN12617000047392.aspx
Study type:  Observational
Study design:   
Phase: 
Countries of recruitment
Contacts
Key inclusion & exclusion criteria
Health Condition(s) or Problem(s) studied
Water balance disturbance in pediatric surgical patients
Appendicitis
Perioperative hyponatremia in pediatric surgical patients.
Stress induced catabolism in pediatric surgical patients
Intervention(s)
All patients with an expected appendicitis is asked for participation in the study. Also, parents are asked. The study period extends from inclusion to the end of the surgical procedure. Blood samples (3 ml) for the determination of blood gas (including sodium concentration), urea, osmolality, ketones, creatinine, cortisol, ADH, aldosterone and renin are taken at the emergency department by a specialist nurse (in addition to the routine samples) and at the end of surgery by a anaesthetic nurse. After induction of anesthesia a blood sample of blood gas and ketones (0,4 ml) is also taken. In addition, urine production is noted and samples are taken for the determination of osmolality, the concentrations of sodium, potassium, creatinine and urea. All the patients are fasted as part of the clinical routines. The volume of all given intravenous fluids during the study period are recorded. Hence the patients are given the normal clinical routines, the interventions are extra blood sampling and sampling from urine. The given fluid and the and the urine output are also recorded.

Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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