Expired Study
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St. Louis, Missouri 63141


Purpose:

Major microvascular blood flow alterations have been documented in patients with severe sepsis. It was also demonstrated that the microcirculation improved in survivors of septic shock but failed to do so in patients dying from acute circulatory failure or with multiple organ failure after shock resolution. Early, effective fluid resuscitation is a key component in the management of patients with severe sepsis and septic shock with the goal of improving tissue perfusion. The best fluid in this early resuscitation phase has been and still is under debate. The aim of this study is to evaluate the effect of Three different Fluids(Albumin 5%, Normal Saline, HES 130 kD) on microcirculation in severe sepsis/septic shock patients using Sidestream Dark Field (SDF) Microscopy and Near-Infrared Spectroscopy (NIRS) analysis.


Criteria:

Inclusion Criteria: - Adult patients will be enrolled within 24 hrs of onset of severe sepsis/septic shock with an indication for fluid bolus administration. Exclusion Criteria: - Liver cirrhosis - shock from other causes - Oral injuries (precluding SDF imaging) - Severe peripheral vascular disease, dialysis fistula, or mastectomies precluding safe forearm occlusion - Age < 18 years


NCT ID:

NCT01319630


Primary Contact:

Principal Investigator
Farid G Sadaka, MD
Mercy Hospital St. Louis


Backup Contact:

N/A


Location Contact:

St. Louis, Missouri 63141
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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