Fluid Resuscitation Optimization in Surgical Trauma Patients (FROST)

NAUnknownINTERVENTIONAL
Enrollment

196

Participants

Timeline

Start Date

December 31, 2015

Primary Completion Date

December 31, 2018

Study Completion Date

December 31, 2019

Conditions
Critical IllnessTrauma
Interventions
DEVICE

FloTrac™ and EV1000™

Interventions to improve cardiovascular performance will be made in all patients whose cardiovascular function is sub-optimal in accordance with routine clinical management during trauma resuscitation. Patients who meet inclusion criteria will be assigned to the intervention or control arm of the study based on the process outlined in the protocol. Patients assigned to the intervention arm will have intra-operative hemodynamic monitoring performed by the anesthesia staff and cardiovascular interventions will be based off of the algorithm described in the protocol. Members of anesthesia or the surgical team can initiate interventions as indicated during routine ICU care or intra-operatively.

Trial Locations (1)

25301

RECRUITING

Charleston Area Medical Center, General Hospital, Charleston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Edwards Lifesciences

INDUSTRY

lead

CAMC Health System

OTHER