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Clinical Trials/NCT05231720
NCT05231720
Unknown
Not Applicable

Mannheim Register of Sepsis and Septic Shock

Universitätsmedizin Mannheim2 sites in 1 country500 target enrollmentDecember 3, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Severe Sepsis
Sponsor
Universitätsmedizin Mannheim
Enrollment
500
Locations
2
Primary Endpoint
all-cause mortality
Last Updated
4 years ago

Overview

Brief Summary

The study aims to investigate clinically and prognostically relevant parameters in patients with sepsis and septic shock within a monocentric observational clinical register.

Detailed Description

All consecutive septic patients at the internists intensive care Unit (ICU) at the University of Mannheim are included in the register and follow up during ICU stay and after that. Data of patients' admission status, septic focus, baseline parameters, and comorbidities are collected. Extensive information about echocardiography, electrocardiography, and imaging procedures are included in the register. Laboratory values, microbiological investigations, organ dysfunction and organ replacement therapies, medication, adverse events, and complications were recorded for several days during the ICU stay (days 1, 2,3, 5,7, and 10). Standard scores for critically ill patients were calculated for the day before admission at the ICU if available, and several time points during the ICU stay. The register includes information about the mortality during ICU stay, 30-day mortality, 6-month mortality, and septic patients' 1-year mortality.

Registry
clinicaltrials.gov
Start Date
December 3, 2019
End Date
December 2023
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Michael Behnes

Prof. Dr.

Universitätsmedizin Mannheim

Eligibility Criteria

Inclusion Criteria

  • Sepsis and septic shock according to current guidelines

Exclusion Criteria

  • other forms of shock not associated with an infection

Outcomes

Primary Outcomes

all-cause mortality

Time Frame: 30 days

Secondary Outcomes

  • all-cause mortality(12 months)

Study Sites (2)

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