Outpatient Care Clinical Trial
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 .
Status | Completed |
Enrollment | 20 |
Est. completion date | June 2014 |
Est. primary completion date | June 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 60 Years |
Eligibility |
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 |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Denmark | Department of gynaecology and obstetrics, Herning Hospital | Herning |
Lead Sponsor | Collaborator |
---|---|
Herning Hospital | University of Aarhus |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | the parents' postnatal sense of security (PPSS) | measured by a questionnaire sent to the parents' in the second week after delivery. | the PPSS is measured the second week after delivery | No |
Secondary | ambulation time | ambulation time measured during the first three days after delivery by an accelerometer | three days | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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