Evaluation of two different devices for non-invasive temperature measurement for pediatric cardiac surgery
Not Applicable
- Conditions
- Congenital heart defectsAdults with congenital heart defects
- Registration Number
- DRKS00010720
- Lead Sponsor
- Zentrum für Anästhesiologie, Rettungs- und Intensivmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
patients aged 0 - 50 years
male or female
ASA I-IV
Anesthesia with flunitrazepam, midazolam, sufentanil, rocuronium, or sevoflurane
Exclusion Criteria
ASA V
Hypo- or hyperthyroid status
fever
pregnancy
known allergies to lunitrazepam, midazolam, sufentanil, rocuronium, or sevoflurane
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of the time course of body core temperature during cardiopulmonary bypass with different invasive and non-invasive measurements methods
- Secondary Outcome Measures
Name Time Method precision and accuracy of non-invasive temperature measurement methods compared to invasive measurement methods