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Trauma clinical trials

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NCT ID: NCT00468507 Completed - Trauma Clinical Trials

The Anti-inflammatory Effects of High-fat Nutrition; Towards a Clinical Application

Start date: March 2007
Phase: Phase 0
Study type: Interventional

Patients undergoing major surgery, trauma and burns are prone to develop an exacerbated inflammatory response, which is potentially lethal to the individual. Recently our group demonstrated that administration of high fat feeding prior to hemorrhagic shock attenuates severe inflammation, gut barrier loss and hepatic damage. High fat feeding releases cholecystokinin in the gut, which stimulates the autonomous nervous system and subsequently activates the efferent vagus nerve. The activated efferent fibers inhibit tissue macrophages via binding of acetylcholine to the alpha7-nicotinergic receptor. In this study the cholecystokinin release in healthy volunteers is monitored in response to low fat and high fat food products.

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: NCT00459160 Recruiting - Trauma Clinical Trials

A Comparison of Two Target Mean Arterial Pressures in the Resuscitation of Hypotensive Trauma Patients

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

The goal of this study will be to determine if a lower than normal blood pressure during surgery for bleeding in the abdomen or chest will result in decreased bleeding and decreased chance of death.

NCT ID: NCT00441792 Completed - Sepsis Clinical Trials

The Effect of Etomidate on Patient Outcomes After Single Bolus Doses

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

The primary aim is to determine the difference in hospital length of stay between septic patients given etomidate and those given midazolam for induction during rapid sequence intubation (RSI) in the emergency department. To achieve this aim we plan to perform a prospective randomized trial measuring the length of stay of patients meeting sepsis criteria and requiring intubation. The investigators will compare in-hospital mortality rates between patients given etomidate and patients given midazolam for induction. In addition to hospital length of stay, secondary endpoints between the two groups will include length of stay in the intensive care unit, death within 48 hours of admission, and total number of days intubated. Research Hypothesis: In adult patients presenting to the emergency department with sepsis and requiring rapid sequence intubation, the length of stay of patients given etomidate will be greater than that of patients given the alternative agent midazolam for induction.

NCT ID: NCT00426972 Completed - Trauma Clinical Trials

Trial of Zesteem (Estradiol) in Healing of Split Thickness Skin Graft Donor Sites

Start date: January 2007
Phase: Phase 3
Study type: Interventional

This trial will assess the effects of Zesteem (estradiol) on the healing of split thickness skin graft donor sites in patients aged 18-85 years.

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.

NCT ID: NCT00356187 Terminated - Trauma Clinical Trials

Beta Blockade in Critical Injury

Start date: February 15, 2006
Phase: Phase 2
Study type: Interventional

Critically injured patients endure a period of hypermetabolism/catabolism after being resuscitated. The metabolic cost of this may be measured in loss of lean body mass, poor wound healing, susceptibility to infection and long hospital stays. While there have been some data to suggest that hypermetabolism can be ameliorated in burn patients by beta blockade, to our knowledge, a prospective trial in trauma patients has not yet been done. Our hypothesis is that nonselective beta blockade will reduce catabolism, improve glucose control, blunt loss of lean body mass, decrease infections and improve outcome in a cohort of critically injured patients.

NCT ID: NCT00328341 Terminated - Clinical trials for Traumatic Brain Injury

The Use of Tissue Oxygen Monitoring in Critically Injured Patients

Start date: April 2006
Phase: N/A
Study type: Observational

It is anticipated that the use of tissue oxygen monitoring to measure brain tissue oxygen and deltoid muscle oxygen will provide more precise information about focal brain ischemia and systemic hypoperfusion than current techniques and measures such as blood pressure, heart rate and intracranial pressure. Understanding the relationship between tissue oxygen tension collected from the brain and deltoid muscle in critically injured patients could lead to a broader understanding of the important metabolic and cellular events that occur following severe injury and the changes induced by therapeutic interventions. Furthermore, the use of interventions designed to improve tissue hypoxia, as measured by low brain or muscle tissue oxygen, may improve mortality or neurological recovery after systemic trauma or head trauma compared to current approaches that do not involve tissue metabolic monitoring.

NCT ID: NCT00323570 Withdrawn - Trauma Clinical Trials

Evaluation of Recombinant Factor VIIa in Patients With Severe Bleeding Due to Trauma

Start date: May 2006
Phase: Phase 3
Study type: Interventional

This trial is conducted in the United States of America (USA). The purpose of this study is to evaluate the treatment of Recombinant Faction VIIa in Patients with Severe Bleeding Due to Trauma Please note that this trial and trial F7TRAUMA-1711 (NCT00184548) have been merged.

NCT ID: NCT00320437 Not yet recruiting - Anxiety Clinical Trials

Intergenerational Transmission of Terror

Start date: May 2007
Phase: Phase 1
Study type: Observational

Our aim is examine avenues by which mothers can transmit their trauma to their children.