CompletedNot Applicable

Relationship of Cerebral Perfusion Pressure Variability to Sepsis-associated Encephalopathy

China110 participantsStarted 2014-05

Plain-language summary

The purpose of the study is to evaluate whether variability of CPP (cerebral perfusion pressure) is related to sepsis-associated encephalopathy and outcomes of patients with sepsis.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * clinical symptoms of sepsis, severe sepsis and septic shock * age over 18 years Exclusion Criteria: * preexisting Neurological diseases * traumatic brain injury * intracranial infectious disease * severe hepatic or renal dysfunction * ICU discharge Within 72 hours * pregnancy

What they're measuring

relationship between cerebral perfusion pressure variability and sepsis-associated encephalopathy

Timeframe: cerebral perfusion pressure is assessed up to 72 hours

Trial details

NCT IDNCT02288715

SponsorKang Yan

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2015-03

View on ClinicalTrials.gov More Sepsis trials