Preventing preterm birth: Costs and effects of screening of healthy women with a singleton pregnancy for a short cervical length.

Phase 3

• Conditions: short cervical length; threatened preterm birth; 10010273

• Registration Number: NL-OMON35507
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 1920

Inclusion Criteria

- capacitated women
- at least 18 years old
- healthy singleton pregnancy
- both measurements of cervical length were < 30 mm (Triple P screening study)

Exclusion Criteria

- major foetal abnormalities
- painful regular uterine contractions
- a history of ruptured membranes
- cervical cerclage
- a previous preterm birth

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Bad neonatal outcome.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>-- delivery before 34 weeks<br /><br>-- child health, growth and development at 2 years time to delivery<br /><br>-- preterm birth rate before 32 weeks, and before 37 weeks<br /><br>-- days of neonatal admission<br /><br>-- maternal morbidity<br /><br>-- maternal admission for preterm labour<br /><br>-- costs</p><br>