Evaluation of two different devices for non-invasive temperature measurement for pediatric cardiac surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00010720

Enrollment

Registered

2016-08-03

Start date

2016-06-21

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

Congenital heart defectsAdults with congenital heart defects

Interventions

Group 1: In all patients body core temperature is measured with different invasive and non-invasive measurement methods. Non-invasive: SpotOn©- and Tcore©-sensors are self adheasive sensors (similar t

Eligibility

Sex/Gender

All

Age

No minimum to 50 Years

Inclusion criteria

Inclusion criteria: patients aged 0 - 50 years male or female ASA I-IV Anesthesia with flunitrazepam, midazolam, sufentanil, rocuronium, or sevoflurane

Exclusion criteria

Exclusion criteria: ASA V Hypo- or hyperthyroid status fever pregnancy known allergies to lunitrazepam, midazolam, sufentanil, rocuronium, or sevoflurane

Design outcomes

Primary

Measure	Time frame
Comparison of the time course of body core temperature during cardiopulmonary bypass with different invasive and non-invasive measurements methods	—

Secondary

Measure	Time frame
precision and accuracy of non-invasive temperature measurement methods compared to invasive measurement methods	—

Countries

Germany

Contacts

Public ContactIvo Brandes

Universitätsmedizin Göttingen, Klinik für Anästhesiologie

ivo.brandes@med.uni-goettingen.de+49 551 3967767

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 5, 2026