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Fast-track Discharge After Elective Cesarean Section

Fast-track Discharge After Elective Cesarean Section

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02911727
Enrollment
142
Registered
2016-09-22
Start date
2016-10-31
Completion date
2020-05-31
Last updated
2020-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Period

Keywords

Cesarean section, Postnatal Care

Brief summary

Cesarean section (CS) is a procedure with prolonged hospital stay compared to the routine for normal vaginal delivery in multiparas. The difference is caused mainly by postoperative pain but improvements in management of pain may change this situation and make early discharge possible. However, several aspects need to be considered. The aim of this project is to evaluate fast-track discharge for multiparas after elective CS concerning neonatal and maternal complications as well as the parents' sense of security and well-being. The study is a randomized controlled trial including 142 women allocated to either 1) the intention to discharge within 28 hours followed by a home visit or 2) standard discharge after at least 48 hours after elective CS. This study will be among the first evaluating fast-track discharge after CS in a European context. If a positive outcome is achieved, we expect that fast-track discharge can be implemented with improved quality and reduced costs in postnatal care following elective CS.

Interventions

PROCEDUREFast-track discharge

As described above

Sponsors

Herning Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Planned elective CS of multiparous women * Singleton pregnancy * Gestational age at least 37+0 weeks * Prepregnancy BMI \<35

Exclusion criteria

* Lack of consent * Women with no or little understanding of and ability to speak Danish * Expected maternal or neonatal complications after delivery

Design outcomes

Primary

MeasureTime frameDescription
Parents' Postnatal Sense of SecurityMeasured one week after deliveryUsing the validated PPSS-questionaire

Secondary

MeasureTime frameDescription
Use of analgesiaDuring the first week postpartumDaily consumption in mg of paracetamol, NSAID and opioid.
Mobilization5 days postpartumStep count measured by an activity monitor (Fitbit Flex)
Breastfeeding6 months after deliveryDuration and extent of breastfeeding
Pain scoresDuring the first week postpartumMeasured by the patient in a questionnaire using numeric rating scale
Surgical complications28 days postpartumNumber of complications using the Clavien-Dindo Classification (1-5)
Complications in the postnatal period28 days postpartumNumber and type of complications using the ICD-10 classification
Contacts to the health care system28 days postpartumNumber of contacts and site of contacts (primary or secondary care)
Readmissions28 days postpartumNumber of readmissions and length of hospital stay in number of days

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026