Hemodynamic Monitoring in fluid Management of ICU patients - PLR & USCOM - PiCCO - TTE

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00022172

Enrollment

Registered

2020-08-24

Start date

2019-12-01

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

A41.9 R57.2

Interventions

Group 1: volume trial via PLR, verification of the result via fluid Bolus, comparison of TTE, PiCCO, USCOM

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: (septic) shock

Exclusion criteria

Exclusion criteria: impossibility of USCOM-measurement due to a new tracheostomy, disagreement

Design outcomes

Primary

Measure	Time frame
Correlation of stroke volume (SV) measured with USCOM vs PiCCO vs Echokardiographie after PLR and volume Trial with 500 ml of saline solution	—

Secondary

Measure	Time frame
Several values like CO/CI, SVV, SVRI, lactate, vasopressor support, VCI diameter, blood pressure (sys., dia., MAP), diuresis	—

Countries

Germany

Contacts

Public ContactStephanie-Susanne Stecher

Medizinische Klinik und Poliklinik IIInterdisziplinär internistische Intensivstation

StephanieSusanne.Stecher@med.uni-muenchen.de089-4400 75836

Outcome results

None listed

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