Accuracy of the measurement of transcutaneous CO2 in the internal emergency Department

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00016906

Enrollment

Registered

2019-05-06

Start date

2019-01-01

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

Ventilated Patients, independent of their disease

Interventions

Group 1: Ventilated patients which get inpatient treatment at the Intermediate Care Station or the emergency department of the internal medicine receive arterial blood gas analysis and transcutaneous

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Ventilated patients which get inpatient treatment at the Intermediate Care Station or the emergency department of the internal medicine.

Exclusion criteria

Exclusion criteria: Non-agreement to the study, Non-ability to express opinion (reduced mental abilities, reduced vigilance, dementia), No possibility to get signal of electrode, medical reasons which disable a measurement, Glasgow-Coma-Scale < 10 P

Design outcomes

Primary

Measure	Time frame
Comparison of transcutaneous und arterial blood gas analysis.	—

Secondary

Measure	Time frame
Evaluation of the transcutaneous CO2-measurement additionally or as replacement to arterial blood gas analysis. Especially concerning diseases and pre-existing diseases of the patients.	—

Countries

Germany

Contacts

Public ContactMartin Müller

Universitätsklinikum Ulm, Kliniken am oberen Eselsberg

info.allgemein@uniklinik-ulm.de07315000

Outcome results

None listed

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