Advanced Perioperative Hemodynamic Monitoring and Clinical Outcome

Not Applicable

• Conditions: R57; Shock, not elsewhere classified

• Registration Number: DRKS00034336
• Lead Sponsor: niklinik Köln

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-05-27
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

Patients undergoing operations or interventions with anaesthesiological participation
Patients receiving advanced hemodynamic monitoring
informed consent for participation

Exclusion Criteria

refusal to participate in the study
contraindications for hemodynamic monitoring via electrical cardiometry

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
cardiac output (CO) obtained by electrical cardiometry (ICON®), FloTrac®, ClearSight®, PiCCO®, TTE/TEE and pulmonary catheter

Secondary Outcome Measures

Name	Time	Method
other hemodynamic parameters: cardiac index (CI), stroke volume (SV), stroke volume index (SVI), systemic vascularresistance (SVR), systemic vascular resistance index (SVRI), hypotension prediction index (HPI)<br> perioperative mortality<br>perioperative organ dysfunction: major cardiac events (MACCE), acute kidney injury, delirium<br>postoperative infection<br>postoperative ICU-admissions<br>length of ICU-stay<br>length-of mechanical ventilation<br>length of hospital stay