Hypothermia in Cesarean Sectio Patients in Regional Anaesthesia
NCT ID: NCT03730090
Last Updated: 2018-11-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
40 participants
OBSERVATIONAL
2018-11-30
2019-12-31
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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zero flux skin termometer
Core temperature is monitored continously, non-invasively
Eligibility Criteria
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Inclusion Criteria
* planned spinal anaesthesia
Exclusion Criteria
* allergy to temperature probe (adhesive)
18 Years
FEMALE
No
Sponsors
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Oslo University Hospital
OTHER
Responsible Party
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Johan C Ræder
Professor
Other Identifiers
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Hypothermia Sectio OUS
Identifier Type: -
Identifier Source: org_study_id
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