Prospective, single-center, open clinical trial to compare two non-calibrated systems for the continuous measurement of cardiac output and stroke volume variation (LiDCO rapid®, ICON®) with a calibrated system using Thermodilutionin (PiCCO®) in adult cardiac surgical patients.

Not Applicable

Completed

• Conditions: Diseases that make a determination of cardiac output and stroke volume variation necessary; I97; Postprocedural disorders of circulatory system, not elsewhere classified

• Registration Number: DRKS00005582
• Lead Sponsor: Klinik für Anästhesiologie, operative Intensivmedizin und SchmerztherapieHelios Klinikum Krefeld

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-01-14
• Study Completion: 2015-11-28
• Last Update Posted: 2024-08-19

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• Planned determination of cardiac output (CO) and stroke volume variation (SVV) by a monitoring procedure in adult cardiac surgical patients.
• Written consent of the patient.

Exclusion Criteria

• Absolute arrhythmia.
• Spontaneous breathing.
• ASA> 4
• infections or skin diseases in the area of possible puncture sites.
• Participation in another interventional clinical trials.
• diseases or disorders that makes the participation in this clinical trial not possible in the opinion of the investigator (support systems in operation (IABP, MECC), hemodynamic instability, catecholamine therapy).

Study & Design

• Study Type: interventional
• Study Design: Not specified