Long-term Cognitive and Cerebral Changes in Sepsis Survivors and Their Predictors

NCT02339649 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 308

Last updated 2017-08-01

No results posted yet for this study

Summary

The main goals of this study are to provide a cognitive, neurological, brain morphological, and serological profile of sepsis survivors in order to make long-term prognosis of recovery and estimate the need for rehabilitation measures in order to help patients reintegrate into normal daily life.

Conditions

  • Severe Sepsis With Septic Shock
  • Severe Sepsis Without Septic Shock

Interventions

PROCEDURE

Blood Sample

Blood Sample

BEHAVIORAL

Neurocognitive Assessment

Neurocognitive Assessment

OTHER

Resting State EEG

10-20 Minutes of Resting State EEG

PROCEDURE

Lumbar Puncture

Lumbar Puncture

OTHER

MRI

60 Minutes MRI

Sponsors & Collaborators

  • University Hospital, Bonn

    collaborator OTHER
  • German Center for Neurodegenerative Diseases (DZNE)

    lead OTHER

Principal Investigators

  • Michael T Heneka, M.D. · German Center for Neurodegenerative Diseases (DZNE)

  • Andreas Hoeft, M.D. · Department of Anesthesiology and Intensive Care Medicine, University Hospital Bonn

  • Christian Putensen, M.D. · Research Unit Pulmonary Dysfunction and Sepsis, Department of Anesthesiology and Intensive Care Medicine, University Hospital Bonn

  • Thomas Klockgether, M.D. · German Center for Neurodegenerative Diseases (DZNE)

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2017-10-31
Completion
2019-10-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02339649 on ClinicalTrials.gov