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Hypothermia in Cesarean Sectio Patients in Regional Anaesthesia

NCT03730090 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2018-11-05

No results posted yet for this study

Summary

To study the core temperature perioperatively in patients due for elective cesarean sectio in spinal anaesthesia.

Core temperature will be registered by a zero-flux (SpotOn. 3m) probe on the forehead, starting in the holding area and continued until normotemperature post-operatively.

Conditions

  • Cesarean Section

Interventions

DEVICE

zero flux skin termometer

Core temperature is monitored continously, non-invasively

Sponsors & Collaborators

  • Oslo University Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-30
Primary Completion
2019-03-31
Completion
2019-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03730090 on ClinicalTrials.gov