Evaluation of a non-invasive method to measure body core temperature with SpotOn® vs. vesical and blood temperature in ICU patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00015482

Enrollment

Registered

2018-09-20

Start date

2018-10-24

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

R68 T88.5

Interventions

Group 1: In ICU patients the invasively measured temperature (blood and/or vesical) will be compared to the temperature measured with the non-invasive SpotOn®-system. The data will be recorded hourly.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients on the ICU aged > 18 years, where temperature measurement in the blood and in the bladder has been established. Informed or deffered consent.

Exclusion criteria

Exclusion criteria: Pregnancy; Not willing to participate in the study for any reasons

Design outcomes

Primary

Measure	Time frame
Every hour the temperature measurement in the blood, in the bladder and with the new SpotOn® system is recorded.	—

Countries

Germany

Contacts

Public ContactAnselm Bräuer

Klinik für Anästhesiologie

abraeue@gwdg.de+49 551 3967767

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 24, 2026