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Trauma clinical trials

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NCT ID: NCT01838863 Terminated - Trauma Clinical Trials

Control of Major Bleeding After Trauma Study

COMBAT
Start date: April 7, 2014
Phase: Phase 2
Study type: Interventional

Bleeding is the most avoidable cause of death in trauma patients. Up to one-third of severely injured trauma patients are found to be coagulopathic and forty percent of the mortality following severe injury is due to uncontrollable hemorrhage in the setting of coagulopathy. It has been established that early administration of fresh frozen plasma decreases mortality following severe injury, replacing lost coagulation factors, improving the coagulopathy and restoring blood volume. This study will determine if giving plasma to severely injured trauma patients during ambulance transport versus after arrival to the hospital will help reduce hemorrhage, thus decreasing both total blood product administration and mortality.

NCT ID: NCT01809899 Terminated - Trauma Clinical Trials

Enhanced Consent for Symptom Provocation Research

Start date: April 2009
Phase: N/A
Study type: Interventional

The overall goal of the proposed study is to insure the protection and safety of human subjects who have been previously exposed to interpersonal traumatic events and who are participants in symptom provocation research. The investigators intend to examine trauma history, cognitive, interpersonal, and genetic predictors of participants' unfavorable reaction to participation in research involving trauma-related script-driven imagery (SDI). The design includes comparing participants in a consent as usual group to participants in an enhanced consent group to see which minimizes unfavorable effects of participating in a research provocation study. In addition, the two different consent groups will be assessed for their effects on psychobiological and neurobiological stress response. Furthermore, the investigators will examine the relationship between the psychobiological responses and neural mechanism during SDI, and unfavorable reactions to participation in symptom provocation research.

NCT ID: NCT01653977 Terminated - Surgery Clinical Trials

Impact of Early Goal-directed Fluid Therapy in Hypovolemic Patients Undergoing Emergency Surgery

Start date: February 2010
Phase: N/A
Study type: Interventional

This study compares the safety and efficacy of GDTs using standard pressure-related parameters vs. dynamic hemodynamic indices associated with fluid compartment monitoring, in trauma patients requiring emergency surgery.

NCT ID: NCT01279369 Terminated - Pregnancy Related Clinical Trials

The Use of Fetal Fibronectin to Predict Delivery Due to Abruptio Placenta

Start date: October 2009
Phase:
Study type: Observational

The purpose of this study is to determine if the presence of fetal fibronectin in the cervicovaginal secretions of pregnant patients with minor maternal trauma predicts impending preterm delivery due to abruptio placenta.

NCT ID: NCT01275976 Terminated - Sepsis Clinical Trials

Effect of C1-esterase Inhibitor on Systemic Inflammation in Trauma Patients With a Femur or Pelvic Fracture

CAESAR
Start date: April 2012
Phase: Phase 3
Study type: Interventional

Trauma and major operation are associated with an excessive inflammation reaction due to tissue injury. This overwhelming immune response is considered to be a major risk factor in the pathogenesis of late inflammatory complications such as acute respiratory distress syndrome (ARDS), multiple organ dysfunction syndrome (MODS) and sepsis. The investigators hypothesize that administration of C1-esterase inhibitor (C1-INH) will attenuate the humane inflammatory response and, thereby, reduce the risk of inflammatory complications due to surgical interventions in trauma patients with a femur or pelvic fracture

NCT ID: NCT00891085 Terminated - Trauma Clinical Trials

Synchronized Intermittent Mechanical Ventilation Versus Open Lung Ventilation With Spontaneous Respiration

SOLV
Start date: October 2007
Phase:
Study type: Observational

The purpose of this study is to collect data on patients who are on breathing machines (ventilators) in the Trauma Surgical Intensive Care Unit (TSICU). This data may help us to determine if one form of assisted breathing is better than another. The two forms of assisted breathing being compared in this study are called BiVent and SIMV. (7) BiVent and SIMV are both delivered by a ventilator but differ in how they assist breathing. SIMV is an older form of mechanical breathing that blows air into the lungs to inflate the lungs. BiVent is a newer form of mechanical ventilation that permits the patient to pull air into the lungs as we normally do. Both BiVent and SIMV are currently being used on a regular basis in the TSICU. The investigators hope that this study will determine if one method of assisted breathing is better than another in preventing complications associated with mechanically assisted breathing.

NCT ID: NCT00833287 Terminated - Obesity Clinical Trials

Immunoregulatory Dysfunction in Trauma Patients: Role of Obesity

ObesityRole
Start date: November 2008
Phase: N/A
Study type: Observational

Patient who have major traumatic injury are at risk to develop postoperative inflammatory complications such as pneumonia and lung trouble called adult respiratory distress syndrome (ARDS). This study will draw blood from trauma patients are several time points after their injury to see if we can predict who is at greatest risk for developing pneumonia or ARDS based upon the results of these immune lab tests. We are particularly interested to see if this will be useful in obese patients who have a greater risk of these post trauma complications

NCT ID: NCT00515736 Terminated - Trauma Clinical Trials

Impact Of Antioxidant Micronutrients On Intensive Care Unit (ICU) Outcome

Etude-AOX
Start date: January 2003
Phase: Phase 3
Study type: Interventional

Critically ill patients are generally exposed to an increased oxidative stress, which is proportional to the severity of their condition. Endogenous antioxidant (AOX) defenses are depleted particularly in those patients with intense inflammatory response. The hypothesis tested is that early I:V: administration of a combination of AOX micronutrient supplements (Se, Zn, Vit C, Vit E, Vit B1) would improve clinical outcome in selected critically ill patients, by reinforcing the endogenous AOX defenses and reducing organ failure.

NCT ID: NCT00464386 Terminated - Trauma Clinical Trials

Continuous Glucose Monitoring (POC) in the ICU

POC
Start date: September 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to prospectively evaluate whether the addition of continuous glucose monitoring to point-of-care (POC) glucometer monitoring improves glucose control.

NCT ID: NCT00421941 Terminated - Trauma Clinical Trials

Enteral Feeding Study of Formula Containing Fish Oil in Critical Care Setting

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the clinical applicability of an enteral tube feeding formula containing fish oil and prebiotics in a critical care population.