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Clinical Trials/DRKS00025762
DRKS00025762
Completed
Not Applicable

The effect of personalized perioperative blood pressure management on intraoperative cerebral oxygen saturation, burst suppression ratio and postoperative neurological outcomes in patients having major surgery: an observational substudy of the IMPROVE-pilot trial

Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf0 sites55 target enrollmentDecember 3, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
euromonitoring and postoperative neurological outcome in patients participating in the IMPROVE pilot trial which investigates intraoperative personalized blood pressure managment
Sponsor
Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf
Enrollment
55
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 3, 2021
End Date
December 24, 2022
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf

Eligibility Criteria

Inclusion Criteria

  • \- American Society of Anesthesiologists physical status class (ASA) II\-IV
  • \- scheduled for elective major surgery under general anesthesia
  • \- surgery expected to last \= 120 minutes

Exclusion Criteria

  • \- emergency surgery
  • \- patients having liver or kidney transplantation
  • \- pregnancy
  • \- status of post transplantation of kidney, liver, heart, or lung
  • \- sepsis (according to current Sepsis\-3 definition)
  • \- impossibility of preoperative automated blood pressure monitoring
  • \- MAP differences between the right and the left arm of more than 20 mmHg surgery that requires controlled hypotension

Outcomes

Primary Outcomes

Not specified

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