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NCT05396417 Clinical Trial

How Well do the Current Cesarean Deliveries Adhere to the Published ERAS Guidelines?

Cesarean Section Complications Clinical Trial

Official title:
Early Recovery After Surgery for Patients Undergoing Cesarean Delivery; Adherence to the Institutional Guideline

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT05396417
Other study ID # Tutkimussuunnitelma25032022_I
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date July 31, 2023

Study information
Verified date April 2023
Source Women's Hospital HUS
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Local guidelines for the postoperative care of women who have undergone cesarean delivery at the HUS/Women's hospital are based recommendations by the ERAS society. This study will take a prospective sample of 500 parturients who have gone through a cesarean delivery and their care will be verified against the local check-list for cesarean delivery.

Description:

The study will produce a snapshot of the current state of treatment in the third largest delivery hospital in Europe. The study will include cesarean deliveries in all urgency categories. 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.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 500
Est. completion date July 31, 2023
Est. primary completion date July 31, 2023
Accepts healthy volunteers
Gender Female
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - Eligible for ERAS protocol cesarean delivery - Cesarean delivery for any indication - Any anesthesia method - Any urgency category Exclusion Criteria: - Age under 18 years

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• cesarean delivery
Cesarean delivery under any form of anesthesia for any reason and for any indication

Locations
Country Name City State
Finland HUS/Women's hospital dept of obstetrics Helsinki

Sponsors (1)
Lead Sponsor Collaborator
Women's Hospital HUS

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Level of adherence to the ERAS guidelines after elective or emergency cesarean delivery To which extent does the postoperative treatment of the parturients meet the ERAS criteria 3 days post surgery
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