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Enhanced recovery after caesarean section.

Enhanced recovery after caesarean section. - Enhanced recovery after caesarean section

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48271
Enrollment
100
Registered
2019-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

voortplantingsstelsel keizersnede caeserean section

Interventions

None listed

Sponsors

Maxima Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Women planned for a caesarean section

Exclusion criteria

Exclusion criteria: - Women who do not speak Dutch - Women younger than 25 years - Women with a history of a midline laparotomy - Women with deep invasive endometriosis - Women with contra-indications for opioids - Total blood loss of 1000cc or more during surgery

Design outcomes

Primary

MeasureTime frame
- Pain measured by a numeric rating scale (NRS) - Use of pain medication - Patient satisfaction measured by a numeric rating scale (NRS) - Length of hospital stay—

Secondary

MeasureTime frame
- operative details - the number of readmissions - postoperative complications (bleeding, wound infection, urinary infection, urinary retention, thrombosis)—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)