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Trauma clinical trials

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NCT ID: NCT02289911 Recruiting - Trauma Clinical Trials

FAST Learning Methods

FAST
Start date: November 2014
Phase: N/A
Study type: Interventional

Training paramedics in new skills via classroom-based teaching has inherent costs and time constraints. The investigators sought to evaluate whether web-based didactics result in similar knowledge improvement and retention of FAST (Focused Assessment with Sonography for Trauma) compared with the traditional method.

NCT ID: NCT02289885 Recruiting - Trauma Clinical Trials

FAST Examination During Emergency Practice

FAST
Start date: November 2014
Phase: N/A
Study type: Interventional

The study evaluates the knowledge, attitude and practice about Focused Assessment with Sonography in Trauma among emergency medicine practitioners in Poland.

NCT ID: NCT02288793 Recruiting - Trauma Clinical Trials

Focused Assessment With Sonography in Trauma

FAST
Start date: November 2014
Phase: N/A
Study type: Observational

The study evaluates the knowledge and attitude about Focused Assessment with Sonography in Trauma examination among medical students and medical staff in Poland.

NCT ID: NCT01812941 Recruiting - Trauma Clinical Trials

Evaluation of Mitochondrial Dysfunction in Severe Burn and Trauma Patients

Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this project is to evaluate the level of mitochondrial dysfunction several patient populations: Burn, trauma, and control group of healthy volunteers. Study hypothesis: Increased plasma concentrations of a newly discovered inflammatory mediated, called mtDNA DAMPS associated with the occurrence of multi-organ dysfunction syndrome in severly injured patients. As the severity of a burn injury or trauma injury increase, so will systemic mitochondrial dysfunction.

NCT ID: NCT01760135 Recruiting - Trauma Clinical Trials

Nutritional Requirement for the Severe Trauma Patients

Start date: November 2012
Phase: Phase 3
Study type: Interventional

After severe trauma, high caloric nutrition supplement do harm on metabolic and immunologic aspects.

NCT ID: NCT01713205 Recruiting - Sepsis Clinical Trials

Prediction Study of Complications After Severe Trauma

PSCAT
Start date: October 2012
Phase:
Study type: Observational

The purpose of this study is to evaluate a clinically and economically most effective diagnostic algorithm for prediction of post-traumatic complications in a multicenter sample of severe trauma patients.

NCT ID: NCT01589107 Recruiting - Surgery Clinical Trials

A Randomized Controlled Trial of a Video Decision Making Aid to Obtain Informed Consent in the Surgical Intensive Care Unit

Start date: December 2011
Phase: N/A
Study type: Interventional

To demonstrate that clinical surrogates of SICU patients who view a video decision aid in addition to receiving written and verbal information about procedures and life sustaining therapy in the SICU make more informed decisions than patients and clinical surrogates who receive written and verbal information alone.

NCT ID: NCT01583010 Recruiting - Trauma Clinical Trials

Improvement of Needle Visibility in Ultrasound Guided Regional Anaesthesia

Start date: December 2011
Phase: N/A
Study type: Interventional

Needle tip visualization, although fundamental to the safety and efficacy of ultrasound-guided regional anesthesia (UGRA), can be extremely challenging. This problem is most marked at steep insertion angles. Studies in patients with UGRA demonstrate that echogenic needle designs have the potential to offer improved visibility and accuracy. Our study pursues another approach. We use (for differentiation) echogenic nerve block needles with ANV®, a new SonoSite software-upgrade (Advanced Needle Visualization Technology®). We will compare UGRA with ANV® against standard UGRA without using this SonoSite software-upgrade. Patients undergoing femoral, supraclavicular or other nerve blocks as part of their routine anesthetic management are included. This work represents the first randomized controlled double blinded clinical trial of ANV® in patients undergoing UGRA. We hypothesize, that we can decrease the time without needle visualization (Loss of needle time in percentage of procedure time) during in-line regional anaesthesia. Furthermore we will record quality of visibility, duration of procedure and insertion angle of the needle.

NCT ID: NCT00882960 Recruiting - Pain Clinical Trials

Intranasal Fentanyl for Pain Management

Start date: April 2009
Phase: Phase 4
Study type: Interventional

Goal of the research will be to demonstrate a reduction in reported pain following the atomization and intra-nasal administration of Fentanyl versus the reduction in pain achieved from intravenous Fentanyl. It is hypothesized that pain should be reduced following fentanyl administration using the intra-nasal atomization equal to the intravenous delivery.

NCT ID: NCT00485927 Recruiting - Stress Clinical Trials

The Effects of Stress on the Clinical Performance of Residents in Simulated Trauma Scenarios

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

Medical practice & training are inherently stressful situations. However, the effects of stress on educational & clinical performance are not well defined. The purpose of the current study is to examine the effects of stress on performance of residents in simulated trauma scenarios. The hypothesis is: 1) acutely stressful scenarios will be appraised as threat by residents and result in elevations of heart rate and salivary cortisol; 2) increased subjective & physiological stress will result in impairments in performance; and 3) greater stress responses will result in greater clinical impairments.