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Clinical Trials/NCT03859726
NCT03859726CompletedNot Applicable

Predictive Value of Sublingual Microcirculation and Peripheral Tissue Oxygen Monitoring in Sepsis Patients With Successful Fluid Resuscitation

Xiangya Hospital of Central South University1 site in 1 country72 target enrollmentStarted: March 20, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
72
Locations
1
Primary Endpoint
Sepsis Related Organ Failure Assessment

Study Overview

Brief Summary

Change and predictive Value of Sublingual Microcirculation and Peripheral Tissue Oxygen Monitoring in Sepsis Patients With Successful Fluid Resuscitation

Detailed Description

Fluid therapy for sepsis patients has always been a research hotspot. Early studies suggest that early goal-directed therapy (EGDT) can reduce mortality in patients with sepsis and septic shock, which is included in the guidelines. However, recent studies suggest that EGDT does not reduce mortality. This may be related to the fact that EGDT only pays attention to systemic circulation and neglects microcirculation.

In the past few decades, arterial blood pressure, blood lactic acid and other circulatory indicators have been the target of septic shock treatment, but normal systemic circulation does not mean normal tissue perfusion. Obstacles to tissue perfusion, oxygenation and microcirculation may still exist. At the same time, compared with systemic hemodynamic parameters, microcirculation parameters may play a stronger role in predicting the prognosis of sepsis patients. It is believed that the ideal goal of resuscitation therapy for sepsis should be based on whether microcirculation function has been restored or not.

Objective

to observe the success rate of microcirculation imaging and oxygen saturation of peripheral tissues in sepsis patients under the guidance of current guidelines and procedures. At the same time, we compared the predictive value of microcirculation indicators to the prognosis of septic shock patients.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • patients fullfilled the diagnostic criteria of Sepsis 3.0

Exclusion Criteria

  • Patients who were younger than 18 years old,
  • pregnant women
  • patients who had been admitted to the Intensive Care Unit(ICU for<24 h)

Outcomes

Primary Outcomes

Sepsis Related Organ Failure Assessment

Time Frame: 72 hours

SOFA

Secondary Outcomes

  • 28-day mortality(28-day)

Investigators

Sponsor
Xiangya Hospital of Central South University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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