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Peri-operative unobtrusive core temperature measurement - clinical pilot trial

Peri-operative unobtrusive core temperature measurement - clinical pilot trial - CoreTemp@OR

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43540
Enrollment
40
Registered
2016-06-15
Start date
2016-07-11
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

chirurgische en medische verrichtingen Core temperature

Interventions

None listed

Sponsors

Philips Research
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult (*18 years) patients planned to undergo surgery with temperature management as standard part of the procedure. These patients are routinely equipped with an oesophageal and/or rectal temperature sensor. (In ETZ bladder sensors are not routinely used).

Exclusion criteria

Exclusion criteria: Exclusion criteria are: neuro-trauma, known pregnancy, prone position during surgery, obesity (BMI>40), and a significant language barrier that prevents the patient from understanding the Informed Consent or answering the questionnaire.

Design outcomes

Primary

MeasureTime frame
Core temp values

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)