Maternal Hypothermia After Caesarean Section - Implications for Postoperative Recovery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Self report questionnaire.
- Who it may be relevant to
- Registry conditions: Caesarean Section. Basic parameters: 18 years — 50 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Norway
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The aim of the study is to assess patient reported outcomes after caesarean section using self report questionnaire.
Detailed description
The project consists of two studies: Study 1 explores patient reported outcomes after caesarean section related to recovery and quality of care. Study 2 explores possible associations between perioperative hypothermia during caesarean section and postoperative infection
Interventions
- Other Self report questionnaire
No intervention
Primary outcome measures
- Patient reported recovery after caesarean delivery and symptoms of post caesarean infection [Time frame: Data collection 24 hours after surgery and 7 days after surgery and 30 days after surgery]
Eligibility criteria
Inclusion Criteria: Caesarean section surgery -
Exclusion Criteria: Stillborn baby, baby admitted to neonatal intensive care,
\-
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Other
Study locations
Norway · 1 center
- Oslo university hospital — Oslo
Identifiers
NCT: NCT07244354 · 911621