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NCT05246969 Clinical Trial

Detecting Sepsis in Patients With Severe Subarachnoideal Hemorrhage

Sepsis Clinical Trial

Official title:
Detecting Sepsis in Patients With Severe Subarachnoideal Hemorrhage

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05246969
Other study ID # Sepsis in SAH
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2017
Est. completion date February 1, 2022

Study information
Verified date March 2022
Source Goethe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 58
Est. completion date February 1, 2022
Est. primary completion date June 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Sepsis detection
The aim of the study was to observe whether the treating physicians were able to detect sepsis by strictly applying the recommended SOFA score.

Locations
Country Name City State
Germany University Hospital Frankfurt Frankfurt Niederrad Hessen

Sponsors (1)
Lead Sponsor Collaborator
Goethe University

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Sepsis SOFA positive Sepsis correctly detected by SOFA score (Sepsis-related organ failure assessment score, 0-24 points) up to 2 months
Primary Sepsis SOFA negative Sepsis not detected by SOFA score (Sepsis-related organ failure assessment score, 0-24 points) up to 2 months
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