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Outpatient Care for Multiparas After Elective Cesarean Section: an Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01921465
Enrollment
20
Registered
2013-08-13
Start date
2013-10-31
Completion date
2014-06-30
Last updated
2016-08-18

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

Conditions

Outpatient Care

Keywords

outpatient care, videoconferencing, elective cesarean section

Brief summary

The purpose of the study is to evaluate whether outpatient cesarean section can be performed in multiparous women without significant decrease in the parents' sense of security .

Interventions

None listed

Sponsors

University of Aarhus
CollaboratorOTHER
Herning Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Planned elective cesarean section of multiparous women * Singleton pregnancy * Age of at least 18 * Gestational age between 37 and 42 weeks * Internet access at home

Exclusion criteria

* Lack of consent * Women with no or little understanding of Danish and ability to speak Danish. * Allergies to medicine included in the pain management regimes * Expected maternal or neonatal complications after delivery * Birth weight of less than 2500 grams

Design outcomes

Primary

MeasureTime frameDescription
the parents' postnatal sense of security (PPSS)the PPSS is measured the second week after deliverymeasured by a questionnaire sent to the parents' in the second week after delivery.

Secondary

MeasureTime frameDescription
ambulation timethree daysambulation time measured during the first three days after delivery by an accelerometer

Countries

Denmark

Outcome results

None listed

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