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Toxemia clinical trials

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NCT ID: NCT01006499 Unknown status - Clinical trials for Sepsis of the Newborn

Role of 'Pentoxifylline and or IgM Enriched Intravenous Immunoglobulin in the Treatment of Neonatal Sepsis'

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

The investigators aim is to investigate whether adjuvant Pentoxifylline , IgM enriched IVIG or Pentoxifylline plus IgM-enriched IVIG reduced mortality from Neonatal sepsis.

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: NCT00979121 Terminated - Sepsis Clinical Trials

Statins for Acutely Injured Lungs From Sepsis

SAILS
Start date: January 2010
Phase: Phase 3
Study type: Interventional

Objective: assess the efficacy and safety of oral rosuvastatin in patients with sepsis-induced Acute Lung Injury (ALI). Hypothesis: Rosuvastatin therapy will improve mortality in patients with sepsis-induced ALI.

NCT ID: NCT00975793 Active, not recruiting - Severe Sepsis Clinical Trials

Australasian Resuscitation In Sepsis Evaluation Randomised Controlled Trial

ARISE
Start date: October 2008
Phase: Phase 3
Study type: Interventional

The ARISE RCT is a multi-centre, randomised, controlled trial of EGDT compared to standard care in patients with severe sepsis presenting to the ED. The study will be conducted in multiple sites with 1600 patients enrolled into the study. Hypothesis to be tested: EGDT, compared to standard Australasian resuscitation practice, reduces 90-day all-cause mortality in patients presenting to the ED with severe sepsis.

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.

NCT ID: NCT00926497 Completed - Sepsis Clinical Trials

Procalcitonin-Guided Decision Making to Shorten Antibiotic Therapy in Suspected Neonatal Early-Onset Sepsis

Start date: June 2005
Phase: N/A
Study type: Interventional

Neonatal bacterial sepsis is a major cause of mortality and morbidity and early antibiotic therapy is crucial for treatment success. Objective: To evaluate the effect of Procalcitonin-guided decision making on duration opf antibiotic therapy in suspected neonatal early-onset sepsis.

NCT ID: NCT00908635 Recruiting - Sepsis Clinical Trials

The Role of Angiopoietin, Tie-2, and Vascular Endothelial Growth Factor (VEGF) in Sepsis-Induced Multiple Organ Dysfunction Syndrome (MODS)

Start date: July 2008
Phase: N/A
Study type: Observational

This study is designated to determine serum concentrations of inflammatory mediators Ang-1, Ang-2, Ang-1/Ang-2 ratio, and Tie-2 in patients with sepsis-induced MODS and to investigate the association among increased permeability, inflammatory mediators, and these serum mediators in development of organ failure.

NCT ID: NCT00889083 Withdrawn - Sepsis Clinical Trials

Hepatic Mitochondrial Function in Sepsis

Start date: April 2009
Phase:
Study type: Observational

Multi-organ failure due to sepsis is a major cause of death in critically ill patients. But the mechanisms leading to this condition are not fully understood. Mitochondrial dysfunction has been shown in skeletal muscle of critically ill septic patients. Liver is very important in sepsis as it is responsible of the synthesis of several inflammatory proteins. Moreover hepatic failure is associated to a bad outcome. The aim of this study is to evaluate the hepatic mitochondrial function in sepsis.

NCT ID: NCT00874367 Completed - Sepsis Clinical Trials

Early-Onset Sepsis Surveillance Study

EOS
Start date: February 2006
Phase: N/A
Study type: Observational

In this observational study, the NICHD Neonatal Research Network (NRN) is conducting surveillance of all infants born at NRN centers to identify all newborns who are diagnosed with early-onset sepsis (EOS) and/or meningitis. The study will: establish current hospital-based rates of EOS among term and preterm infants in the era of intrapartum antibiotic prophylaxis; monitor the organisms associated with EOS and meningitis; compare asymptomatic and symptomatic infants by gestational age and pathogen; and monitor sepsis-associated mortality rates by pathogen group.

NCT ID: NCT00862290 Completed - Sepsis Clinical Trials

Circulating microRNAs as Biomarkers of Sepsis

Start date: August 2008
Phase: N/A
Study type: Observational

MicroRNA has been demonstrated to play a crucial role in regulating cell processes. Recently, microRNA was identified to exist in human serum or plasma, and it might be related to certain diseases. Several microRNAs are involved in sepsis, such as miR-146, miR-155, and so on. But whether serum miR-146 is present in serum of septic patients remains unknown. The present study was designed to identify the existence of specific microRNAs, which might be new markers for sepsis and its prognosis.