Enhanced recovery after caesarean section.

Withdrawn

• Conditions: voortplantingsstelsel keizersnede; caeserean section

• Registration Number: NL-OMON48271
• Lead Sponsor: Maxima Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

Women planned for a caesarean section

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

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>- Pain measured by a numeric rating scale (NRS)<br /><br>- Use of pain medication<br /><br>- Patient satisfaction measured by a numeric rating scale (NRS)<br /><br>- Length of hospital stay </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- operative details<br /><br>- the number of readmissions<br /><br>- postoperative complications (bleeding, wound infection, urinary infection,<br /><br>urinary retention, thrombosis)</p><br>