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Clinical Trials/NCT02185118
NCT02185118
Unknown
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In-vitro Experimental Study About Effects of Subanesthetic Isoflurane/Sevoflurane in 60% Oxygen on Clinical In-vitro Sepsis

Air Force Military Medical University, China1 site in 1 country50 target enrollmentJune 2014

Overview

Phase
N/A
Intervention
oxygen
Conditions
Sepsis
Sponsor
Air Force Military Medical University, China
Enrollment
50
Locations
1
Primary Endpoint
Subcellular location of Nuclear Factor-KAPPA B p65 subunit
Last Updated
11 years ago

Overview

Brief Summary

Sepsis is a major cause of death in intensive care units. Despite the investigators improved understanding, which has reduced the risk of dying with sepsis, the number of people who die each year continues to increase due to an overall increase in the number of cases.In our previous study, the investigators have showed that 100% oxygen or 0.5 minimum alveolar concentration (MAC) isoflurane/sevoflurane in 60% oxygen protect mouse macrophage cell line against in-vitro sepsis induced by lipopolysaccharide (LPS).

In this study, the investigator hypothesized that treatment of 100% oxygen or 0.5 MAC isoflurane/sevoflurane in 60% oxygen protected against clinical in-vitro models of sepsis induced by LPS or plasma from septic patients.

Detailed Description

100% oxygen or 0.5 MAC isoflurane/sevoflurane in 60% oxygen would inhibit increases of tumor necrosis factor (TNF)-alpha, interleukin-1beta, interleukin-6 in the cell culture supernatant after stimulation of LPS or plasma from septic patients, and also inhibit the nuclear location of nuclear factor-kappa B p65 subunit.

Registry
clinicaltrials.gov
Start Date
June 2014
End Date
July 2018
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Air Force Military Medical University, China
Responsible Party
Principal Investigator
Principal Investigator

Lichao Hou

M.D., Ph.D

Air Force Military Medical University, China

Eligibility Criteria

Inclusion Criteria

  • Human PBMCs were only isolated from the adult patients without sepsis/SIRS/infectious diseases.
  • The plasma for induction of clinical in-vitro sepsis, was only isolated from adult patients with sepsis.

Exclusion Criteria

  • Patients who had been selected for other clinical trials in the 3 months before.

Arms & Interventions

oxygen plus isoflurane/sevoflurane

All human peripheral blood mononuclear cells (PBMCs) were from patients with non sepsis/non SIRS/non infection. The above cells were treated with oxygen or oxygen plus isoflurane/sevoflurane after stimulation of lipopolysaccharide/plasma from septic patients.

Intervention: oxygen

oxygen plus isoflurane/sevoflurane

All human peripheral blood mononuclear cells (PBMCs) were from patients with non sepsis/non SIRS/non infection. The above cells were treated with oxygen or oxygen plus isoflurane/sevoflurane after stimulation of lipopolysaccharide/plasma from septic patients.

Intervention: Sevoflurane

oxygen plus isoflurane/sevoflurane

All human peripheral blood mononuclear cells (PBMCs) were from patients with non sepsis/non SIRS/non infection. The above cells were treated with oxygen or oxygen plus isoflurane/sevoflurane after stimulation of lipopolysaccharide/plasma from septic patients.

Intervention: Isoflurane

Outcomes

Primary Outcomes

Subcellular location of Nuclear Factor-KAPPA B p65 subunit

Time Frame: within 10 hours after the intervention

Secondary Outcomes

  • tumor necrosis factor-alpha(within 10 hours after the intervention)
  • interleukin- 1 beta(within 10 hours after the intervention)
  • interleukin 6(within 10 hours after the intervention)

Study Sites (1)

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