Evaluation of esCCO monitoring for continuous, non-invasive measurement of cardiac output

Evaluation of esCCO monitoring for continuous, non-invasive measurement of cardiac output - COKA

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00008769

Enrollment

Registered

2019-02-15

Start date

2016-01-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Q05.9 I50.9

Interventions

Group 1: Method comparison for the measurement of cardiac output by non-invasive esCCO monitoring against transpulmonary thermodilution (PiCCO monitoring) in gynecological patients (pregnant women dur

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: gynecological patients; pregnant women with the indication for a fetoscopic procedure

Exclusion criteria

Exclusion criteria: Age <18 years, atrial fibrillation, pacemaker

Design outcomes

Primary

Measure	Time frame
Comparison of cardiac output measured with the esCCO system compared to measurement with the PiCCO system perioperatively (every 30 minutes until the end of the operation)	—

Secondary

Measure	Time frame
Comparison of heartbeat volume, systemic resistance and possible influencing factors (age, gender, previous illnesses, catecholamine therapy, storage, fluid therapy, respiration) when measuring with the esCCO system versus measurement with the PiCCO system	—

Countries

Germany

Contacts

Public ContactChristian Koch

UKGM Standort Gießen Abteilung für Anaesthesiologie, Operative Intensivmedizin und Schmerztherapie

christian.koch@chiru.med.uni-giessen.de0641-98556622

Outcome results

None listed

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