High Volume Lactated Ringer's Solution and Pancreatitis

PHASE2/PHASE3TerminatedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

January 31, 2016

Study Completion Date

January 31, 2016

Conditions
Pancreatitis
Interventions
OTHER

Administration of Lactated Ringer's (LR) Solution

"Patients will be randomized to low volume or high volume group. Patient in the low volume group will receive fluids via infusion at a rate of 1.5 cc/kg/hr. Fluid administration may be continued through the 90 minute post-procedure observation period. Patients in the high volume group will receive fluids via infusion by the following weight based regimen:~* initial bolus of LR prior to ERCP of 7.5 cc/kg over 1 hour~* LR fluid infusion during the procedure at 5 cc/kg/hr~* Post-procedure bolus of 20 cc/kg over 90 minutes"

Trial Locations (6)

53226

Medical College of Wisconsin, Milwaukee

55446

Minnesota Gastroenterology, Plymouth

60035

NorthShore University HealthSystem, Highland Park

60076

Advocate Health Care, Skokie

60201

NorthShore University HealthSystem, Evanston

84132

University of Utah Health Care, Salt Lake City

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Medical College of Wisconsin

OTHER

collaborator

Allina Health System

OTHER

collaborator

Wake Forest University Health Sciences

OTHER

collaborator

University of Utah

OTHER

lead

Endeavor Health

OTHER