Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Blood Pressure
  • Intraoperative Hypotension
  • Postoperative Complications
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Outcomes Assessor)Masking Description: In control group patients, the treating anesthesiologists are blinded to the data of preoperative automated blood pressure monitoring. Participants and outcomes assessors are blinded to group allocation.Primary Purpose: Treatment

Participation Requirements

Age
Between 45 years and 125 years
Gender
Both males and females

Description

not provided

not provided

Tracking Information

NCT #
NCT04894045
Collaborators
RWTH Aachen University
Investigators
Principal Investigator: Bernd Saugel, Prof. Dr. Department of Anesthesiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany Principal Investigator: Karim Kouz, Dr. Department of Anesthesiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany