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Clinical Trials/NCT02185118
NCT02185118UnknownNot Applicable

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 enrollmentStarted: June 2014Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
50
Locations
1
Primary Endpoint
Subcellular location of Nuclear Factor-KAPPA B p65 subunit

Study 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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Experimental

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 (Drug)

oxygen plus isoflurane/sevoflurane

Experimental

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 (Drug)

oxygen plus isoflurane/sevoflurane

Experimental

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 (Drug)

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)

Investigators

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

Lichao Hou

M.D., Ph.D

Air Force Military Medical University, China

Study Sites (1)

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