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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COMPLETED
20 participants
OBSERVATIONAL
2014-10-31
2016-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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study group
patients undergoing cesarean under epidural anesthesia
novel device
novel device being used to measure shivering
Interventions
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novel device
novel device being used to measure shivering
Eligibility Criteria
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Inclusion Criteria
* epidural in situ
Exclusion Criteria
19 Years
FEMALE
Yes
Sponsors
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University of British Columbia
OTHER
Responsible Party
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Principal Investigators
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Simon Massey, MD FRCPC
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Locations
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BC Women's Hospital
Vancouver, British Columbia, Canada
Countries
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Other Identifiers
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H14-02480
Identifier Type: -
Identifier Source: org_study_id
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