How Well do the Current Cesarean Deliveries Adhere to the Published ERAS Guidelines?
NCT ID: NCT05396417
Last Updated: 2023-04-26
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
500 participants
OBSERVATIONAL
2023-01-01
2023-07-31
Brief Summary
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Detailed Description
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The data will be collected prospectively by enrolling parturients in consecutive order from the study start date. The data will be collected in the form of a paper check list that is to be filled up by the nursing staff and doctors who are taking care of the parturient through her stay at the hospital.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Cesarean delivery
Any urgency any reason
cesarean delivery
Cesarean delivery under any form of anesthesia for any reason and for any indication
Interventions
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cesarean delivery
Cesarean delivery under any form of anesthesia for any reason and for any indication
Eligibility Criteria
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Inclusion Criteria
* Cesarean delivery for any indication
* Any anesthesia method
* Any urgency category
Exclusion Criteria
18 Years
55 Years
FEMALE
No
Sponsors
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Women's Hospital HUS
OTHER
Responsible Party
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Antti Vaananen
Principal investigator
Locations
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HUS/Women's hospital dept of obstetrics
Helsinki, , Finland
Countries
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Other Identifiers
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Tutkimussuunnitelma25032022_I
Identifier Type: -
Identifier Source: org_study_id
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