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Severe Sepsis clinical trials

View clinical trials related to Severe Sepsis.

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NCT ID: NCT00535821 Terminated - Septic Shock Clinical Trials

Minimally-Invasive Cardiovascular Hemodynamic Optimization (MiCHO) Versus Early Goal-Directed Therapy (EGDT) in the Management of Septic Shock

MiCHO
Start date: June 2007
Phase: Phase 4
Study type: Interventional

Early intervention in the treatment of septic shock, including early goal-directed therapy (EGDT) in the first 6 hours of disease presentation, has been shown to significantly decrease mortality. However, this approach requires invasive hemodynamic monitoring, thus limiting its widespread application in the emergency department setting. A minimally invasive protocol utilizing esophageal Doppler monitoring (EDM) may be of benefit and practical if it is shown to result in similar outcome as EGDT.

NCT ID: NCT00534287 Completed - Septic Shock Clinical Trials

Comparison of Two Antibiotic Regimen (Meropenem Versus Meropenem+Moxifloxacin)in the Treatment of Severe Sepsis and Septic Shock

MaxSep
Start date: October 2007
Phase: Phase 3
Study type: Interventional

Severe sepsis and septic shock are diseases of infectious origin with a high risk of death. Antibiotic therapy is mandatory but it is unknown whether one antibiotic alone is sufficient for initial therapy. The purpose of this study is to compare a therapy with meropenem alone or the combination of meropenem plus moxifloxacin in the treatment of severe sepsis/ septic shock. Patients randomly receive one of the two treatments for at least 7 days but not longer than 14 days.

NCT ID: NCT00510835 Active, not recruiting - Sepsis Clinical Trials

Protocolized Care for Early Septic Shock

ProCESS
Start date: March 2008
Phase: N/A
Study type: Interventional

The ProCESS study is large, 5-year, multicenter study of alternative resuscitation strategies for septic shock. The study hypothesizes that there are "golden hours" in the initial management of septic shock where prompt, rigorous, standardized care can improve clinical outcomes.

NCT ID: NCT00484146 Terminated - Severe Sepsis Clinical Trials

Alterations of Immunologic Mediators During Severe Sepsis

LAVISS_01
Start date: June 2006
Phase: N/A
Study type: Observational

Severe sepsis induces significant changes in expression of insulin- and toll-like receptors, cytokines, markers of apoptosis, and activation of t- and b-lymphocytes.

NCT ID: NCT00484133 Recruiting - Severe Sepsis Clinical Trials

Microcirculation Guided Therapy Versus "Standard Treatment" of Severe Sepsis

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to asses the recovery of organ failure between two resuscitation protocols in severe sepsis: standard, pressure guided therapy versus a microcirculation guided therapy

NCT ID: NCT00463645 Completed - Severe Sepsis Clinical Trials

Investigation of Correlation Between Interstitial and Arterial Blood Glucose Concentrations in Septic Patients

Start date: September 2005
Phase: N/A
Study type: Observational

This is a mono-centre trial performed at the medical ICU at the Medical University Graz. There will be a study visit (V1) and a follow-up assessment (V2). In the study visit (V1) arterial blood glucose values will be monitored and subcutaneous sampling of interstitial fluid (ISF) with microdialysis for glucose determination and with microperfusion for cytokine-measurement will be performed. The study visit will last for 26 hours starting with the insertion of two catheters in the abdominal subcutaneous tissue (one microdialysis- and one microperfusion catheter). The primary hypothesis of the study is: Interstitial fluid glucose concentration profiles correlates to the arterial blood glucose concentration profile in patients with severe sepsis in the medical ICU.

NCT ID: NCT00449800 Recruiting - Sepsis Clinical Trials

Pharmacokinetic of Ceftriaxone in Septic ICU Patients

PORTHOS
Start date: July 2006
Phase: Phase 4
Study type: Interventional

Ceftriaxone pharmacokinetics variability in intensive care unit septic patients In intensive care units, drug dosage is often based on study made on healthy volunteers or on less severe patients. However, pharmacokinetic alterations have been described for some drugs used in intensive care units. These alterations, consequences of alteration of volume of distribution, of protein concentrations, of impaired hepatic and renal functions can result in accumulation with toxicity or « under dosage » with inefficacity. Ceftriaxone is an antibiotic often prescribed in intensive care unit. However, despite this large utilisation, very few data is available on the pharmacokinetic in intensive care unit, and optimal dosage is not known. Our objective is to develop a population pharmacokinetics model of ceftriaxone in intensive care unit patients with sepsis, severe sepsis and septic shock and to identify the « data » explaining interindividual variability of each pharmacokinetics parameter.

NCT ID: NCT00448968 Completed - Sepsis Clinical Trials

The Utility of Ischemia Modified Albumin (IMA) in Sepsis

Start date: March 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine if levels of ischemia modified albumin (IMA) in blood are elevated in patients with suspected infection and are predictive of severity of illness in patients with sepsis. In order to compare subjects with infection to those without infection who are representative of the ED population at each site, a group of non-infected control patients will be enrolled. Each hospital will enroll subjects with age (by decade) and sex matched controls to reflect the population of subjects suspected of infection.

NCT ID: NCT00407823 Completed - Septic Shock Clinical Trials

Comparison of Pediatric Septic Shock Treatment With and Without Central Venous Oxygen Saturation Monitoring

Start date: January 2004
Phase: N/A
Study type: Interventional

The purpose of this study was to compare ACCM/PALS guidelines performed with and without central venous oxygen saturation monitoring on the morbidity and mortality rate of children with severe sepsis and septic shock.

NCT ID: NCT00398736 Completed - Septic Shock Clinical Trials

A Non-invasive Approach to the Assessment of Volume Status in Mechanically Ventilated Septic Patients.

Start date: n/a
Phase: Phase 2
Study type: Observational

To evaluate the use of sonographic inferior caval vein assessment in mechanically ventilated septic patients. Volume assessment in mechanically ventilated patients with inflammation is of major importance to guide fluid therapy. The researchers investigated whether measurement of caval vein diameter correlates with invasively assessed volume-based hemodynamic parameters.