Cesarean Section Clinical Trial
Official title:
Hypothermia in Cesarean Sectio Patients in Regional Anaesthesia
Verified date | November 2018 |
Source | Oslo University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Not yet recruiting |
Enrollment | 40 |
Est. completion date | December 2019 |
Est. primary completion date | March 2019 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Elective patients - planned spinal anaesthesia Exclusion Criteria: - Conversion of procedure to general anaesthesia - allergy to temperature probe (adhesive) |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Oslo University Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | incidence of perioperative hypothermia, less than 36.0 degrees | mesured by zero flux in forehead | perioperatively | |
Secondary | patient satisfaction: Patient will be asked to grade | Patient will be asked to grade their feeling of being Cold/warm | perioperatively, repeated | |
Secondary | duration of perioperative hypothermia | number of minutes below 36.0 degrees | perioperatively, continously | |
Secondary | shivering | any shivering due to being cold | perioperatively |
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