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Weaning with central venous oximetry

Weaning with central venous oximetry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00017573
Enrollment
50
Registered
2019-09-24
Start date
2019-09-20
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

J96

Interventions

Group 1: Mechanical ventilated patients who are ready for weaning will be followed up for 96 hours. During the spontaneous breathing trial (one hour) a measuring probe will be placed through a centra

Sponsors

Universitätsklinikum Augsburg, Abteilung für Anästhesiologie und Operative INtensivmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: patients with central venous line, patients ready for extubation, more than 48 hours on mechanical ventilation, no muscle rexaxants 24h bevore begin, hemoglobin >8g/dl, no clinical relevant acidosis, improvement of the reason the patient is ventilated for, temperature 90%, PaO2/FiO2 > 150; PEEP < 10 cm H2O; pressure support < 10 cm H2O

Exclusion criteria

Exclusion criteria: neurosurgical patients, patients under 18 and over 85 years, pregnancy, neuromuscular diseases, patients with tracheostoma.

Design outcomes

Primary

MeasureTime frame
Status of ventilation (extubated vs (re-)intubated) within 96 hours after measurement.

Secondary

MeasureTime frame
28-day-mortality 90-day-mortality Hospital mortality Days outside the intensive care unit (days which patients spent alive and outside of the ICU at day 28 after the spontaneous breathing trial)

Countries

Germany

Contacts

Public ContactUlrich Jaschinski

Universitätsklinikum Augsburg, Abteilung für Anästhesiologie und Operative INtensivmedizin

ulrich.jaschinski@uk-augsburg.de0049(0)8214002311

Outcome results

None listed

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