Comparing the Effects of Lactated Ringers and Normal Saline in Acute Pancreatitis

NACompletedINTERVENTIONAL
Enrollment

79

Participants

Timeline

Start Date

December 31, 2014

Primary Completion Date

October 23, 2020

Study Completion Date

October 23, 2020

Conditions
Pancreatitis
Interventions
OTHER

Fluid Management

The patient will remain NPO for at least the first 24 hours. The following studies will be obtained at the time of admission if not previously obtained in the ED: CMP, GGT, Amylase, Lipase, Triglycerides, CBC, and CRP, along with an abdominal ultrasound. CBC, CRP, BMP, amylase and lipase levels will be obtained at 24 and 48 hours (+/- 2 hours). SIRS status will be evaluated with vital sign checks every 4 hours and the leukocyte counts every 24 hours.

Trial Locations (3)

20010

Children's National Health System, Washington D.C.

23507

Children's Hospital of The King's Daughters, Norfolk

45229

Cincinnati Children's Hospital Medical Center, Cincinnati

All Listed Sponsors
collaborator

Children's National Research Institute

OTHER

collaborator

Children's Hospital of The King's Daughters

OTHER

lead

Children's Hospital Medical Center, Cincinnati

OTHER