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Advanced Perioperative Hemodynamic Monitoring and Clinical Outcome

Advanced Perioperative Hemodynamic Monitoring and Clinical Outcome - AHEMO

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00034336
Enrollment
150
Registered
2024-05-27
Start date
2024-06-28
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

R57

Interventions

Group 1: hemodynamic parameters (CO, MAP, CI, SVRI, SV, SVV, PPV, etc.) obtained by electrical cardiometry (ICON®) and FloTrac® during an operation, procedure and/or stay at on a intensive care unit w

Sponsors

Uniklinik Köln
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

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

Secondary

MeasureTime frame
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) perioperative mortality perioperative organ dysfunction: major cardiac events (MACCE), acute kidney injury, delirium postoperative infection postoperative ICU-admissions length of ICU-stay length-of mechanical ventilation length of hospital stay

Countries

Germany

Contacts

Public ContactTobias Kammerer

Uniklinik Köln

tobias.kammerer@uk-koeln.de+49 221 478-82058

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026