German Lactat Clearance in Severe Sepsis

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01929772

Acronym

GLASS

Enrollment

300

Registered

2013-08-28

Start date

2012-09-30

Completion date

2015-04-30

Last updated

2015-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Septic Shock, Severe Sepsis

Brief summary

The aim of this study is to investigate if there is a correlation between lactate clearance and the course at patients with severe sepsis and septic shock at german intensive care units.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

Healthy volunteers

Inclusion criteria

* Patients with severe sepsis or septic shock * signed informed consent

Exclusion criteria

* severe sepsis or septic schock within 4 weeks before inclusion of study * shock of other genesis * persons being accomondated in an institution because of court or official order * persons being interdependet to the investigator * employees of the investigator

Design outcomes

Primary

Measure	Time frame	Description
Lactate Clearance	Within 6 hours after diagnoses	Determination of lactate clearance within 6 hours after diagnosis of severe sepisis and septic shocik

Secondary

Measure	Time frame
SOFA Score	Day of hospitalization, day 7, day 8

Other

Measure	Time frame	Description
Mortality	After 28 days	Determination of the mortality of the collective after 28 days
Duration intensive care unit and hospitalization	28 days	—

Countries

Germany

Outcome results