Dallas, Texas 75206


Purpose:

This is a randomized controlled trial to compare viscoelastic (VE) guided resuscitation to fixed-ratio resuscitation in trauma patients with hemorrhagic shock on the utilization of blood products, effects on coagulation and inflammatory mediators, and how these strategies affect post resuscitation adverse events.


Study summary:

This is an open labeled study as the VE guided resuscitation will be based on the visible VE results. Aim 1 will compare the number of blood products utilized in each resuscitation strategy. Aim 2 will analyze the coagulation and inflammatory mediators in each resuscitation strategy to determine if there is a difference in the mechanism of coagulopathy. Aim 3 will determine if the different resuscitation strategies have an effect on post resuscitation adverse events.


Criteria:

Inclusion Criteria: 1. Trauma patient 2. MTP Activation 3. Only patients ≥ 14 years old 4. Alive at 31 mins after arrival in ED Exclusion Criteria: 1. Transfer from OSH 2. Received CPR for more than 5 mins 3. Burned 4. Pregnant or Prisoner 5. Known DNR 6. Jehovah's witness


NCT ID:

NCT03765866


Primary Contact:

Principal Investigator
Michael W. Cripps, M.D.
UT Southwestern Medical Center

Michael W. Cripps, M.D.
Phone: 214-648-2708
Email: michael.cripps@utshouthwestern.edu


Backup Contact:

Email: nadia.nassaj@utsouthwestern.edu
Nadia Nassaj, MS
Phone: 214-648-7200


Location Contact:

Dallas, Texas 75206
United States

Michael W Cripps, MD
Phone: 214-648-2708
Email: michael.cripps@utsouthwestern.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

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