Method comparison of cardiac output measurement during extracorporeal membrane oxygenation (veno-venous ECMO) in patients with ARDS

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00028049

Enrollment

Registered

2022-02-08

Start date

2020-11-27

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

J80 I50

Interventions

Group 1: VV ECMO Patients with available hemodynamic montoring via Swan-Ganz catheter and PiCCO.

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1) Patients with VV ECMO support for ARDS and established Swan-Ganz catheter and PiCCO monitoring

Exclusion criteria

Exclusion criteria: 1. pregnancy 2. increased intracranial pressure 3. known, but untreated intracardial shunt (ASD/VSD) 4. contraindications agains transesophageal echocardiography

Design outcomes

Primary

Measure	Time frame
Bias, precision, limits of agreement, concordance and radial concordance between both monitoring approaches and compared to transesophageal echocardiography	—

Secondary

Measure	Time frame
No secondary outcome analysis planned	—

Countries

Germany

Contacts

Public ContactStefan Kreyer

Klinik für Anästhesiologie und Intensivmedizin Universitätsklinikum Bonn

stefan.kreyer@ukbonn.de022828714118

Outcome results

None listed

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