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Clinical Trials/NCT05246969
NCT05246969CompletedNot Applicable

Detecting Sepsis in Patients With Severe Subarachnoideal Hemorrhage

Goethe University1 site in 1 country58 target enrollmentStarted: June 1, 2017Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
58
Locations
1
Primary Endpoint
Sepsis SOFA positive
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The study aims to evaluate the suitability of the SOFA score implemented by the Sepsis 3 guideline to detect sepsis in patients suffering from subrarachnoid hemorrhage.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Retrospective

Eligibility Criteria

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

Inclusion Criteria

  • •Critically ill patients suffering from moderate to severe subarachnoid hemorrhage (WFNS >2).

Exclusion Criteria

  • •children under the age of 18 years Patients with minor subarachnoid hemorrhage < WFNS stage 2.

Outcomes

Primary Outcomes

Sepsis SOFA positive

Time Frame: up to 2 months

Sepsis correctly detected by SOFA score (Sepsis-related organ failure assessment score, 0-24 points)

Sepsis SOFA negative

Time Frame: up to 2 months

Sepsis not detected by SOFA score (Sepsis-related organ failure assessment score, 0-24 points)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Goethe University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Armin N. Flinspach

Principal Investigator

Goethe University

Study Sites (1)

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