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Toxemia clinical trials

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NCT ID: NCT01145560 Completed - Septic Shock Clinical Trials

A Study to Compare the Efficacy and Safety of 2 Dosing Regimens of IV Infusions of AZD9773 (CytoFabâ„¢) With Placebo in Adult Patients With Severe Sepsis and/or Septic Shock

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The primary purpose of this study to evaluate the effect of two different doses of AZD9773 (CytoFabâ„¢) versus placebo on ventilator free days (VFDs) over the first 28 days after the start of dosing with AZD9773 in patients with severe sepsis and/or septic shock, who are already receiving appropriate standard of care treatment for sepsis.

NCT ID: NCT01139489 Completed - Sepsis Clinical Trials

Safety and Efficacy of Procalcitonin Guided Antibiotic Therapy in Adult Intensive Care Units (ICU's)

SAPS
Start date: November 2009
Phase: N/A
Study type: Interventional

This is a randomized controlled trial comparing standard-of-care therapy of infections in critically ill patients with a procalcitonin-guided approach evaluating efficacy (antibiotics consumption) and safety (mortality).

NCT ID: NCT01128283 Completed - Sepsis Clinical Trials

Indicators of Inflammation and Coagulation in Sepsis

Start date: January 2002
Phase: N/A
Study type: Observational

We will collect blood samples from patients with the diagnosis of sepsis and other ICU patients. We will describe the course of different mediator levels and organ injury markers and follow their progression throughout the course of the study.

NCT ID: NCT01120678 Completed - Neonatal Sepsis Clinical Trials

Improved Detection of Neonatal Sepsis Using a Targeted Biomarker Assay

Start date: February 2009
Phase:
Study type: Observational

The purpose of this study is to determine whether analysis of specific serum biomarkers will improve the diagnosis of late onset neonatal sepsis and to determine the correlation between plasma levels of specific cytokines and bacteremia in NICU patients >3 days of age.

NCT ID: NCT01069146 Completed - Sepsis Clinical Trials

Mild Therapeutic Hypothermia During Severe Sepsis

Start date: January 2002
Phase: N/A
Study type: Interventional

Objectives: to evaluate the feasibility, the safety and the effects on physiological parameters of mild therapeutic hypothermia during septic shock. Design: a randomized, controlled, pilot physiological study. Setting: a 15-beds university-affiliated intensive care unit of a teaching Hospital. Patients: twenty ventilated and sedated adults patients with septic shock Intervention: Mild therapeutic hypothermia between 32 and 34°C during 36 consecutive hours using an external water cooling blanket.

NCT ID: NCT01029080 Completed - Sepsis Clinical Trials

Cerebrovascular Autoregulation During Sepsis

Start date: December 2009
Phase: N/A
Study type: Observational

The aim of the study is to correlate the dynamic cerebrovascular autoregulation by patients with sepsis with a sepsis-associated delirium.

NCT ID: NCT01027429 Completed - Sepsis Clinical Trials

Simplified Antibiotic Therapy for Sepsis in Young Infants

SATT
Start date: December 2009
Phase: Phase 3
Study type: Interventional

This trial evaluates primary care clinic-based simplified antibiotic therapy options for young infants, 0-59 days old in high neonatal mortality settings in peri-urban Karachi where hospital referral is frequently refused by families.

NCT ID: NCT01012115 Completed - Sepsis Clinical Trials

Coagulation Factors, Cytokines and Tissue Injury Markers in Sepsis

Histone
Start date: October 2009
Phase: N/A
Study type: Observational

In an effort to better understand the interaction between the different mediators, the investigators propose to examine the time course of mediators, the indexes of organ injury and the coagulation cascade.

NCT ID: NCT00994812 Completed - Infertility Clinical Trials

The Effects of Metformin on Pregnancy and Miscarriage Rates in Polycystic Ovary Syndrome (PCOS)

Start date: August 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether metformin may improve pregnancy rates, and decrease miscarriage rates and complications of pregnancy, such as toxemia and gestational diabetes, in women with polycystic ovary syndrome (PCOS).

NCT ID: NCT00962156 Completed - Septic Shock Clinical Trials

Scandinavian Starch for Severe Sepsis/Septic Shock Trial

6S
Start date: December 2009
Phase: Phase 3
Study type: Interventional

- By tradition hydroxyethyl starch (HES) is used to obtain fast circulatory stabilisation in critically ill. - High molecular weight HES may, however, cause acute kidney failure in patients with severe sepsis. - Now the low molecular weight HES 130/0.4 is the preferred colloid in Scandinavian intensive care units (ICU) and 1st choice fluid for patients with severe sepsis. - HES 130/0.4 is largely unstudied in ICU patients. - This investigator-initiated Scandinavian multicentre trial will be conducted to assess the effects of HES 130/0.4 on mortality and endstage kidney failure in patients with severe sepsis. - The trial will provide important data to all clinicians who resuscitate septic patients.