European Fibronectin Study

Completed

• Conditions: Preterm Labor; 10026908

• Registration Number: NL-OMON37632
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

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

Inclusion Criteria

- Gestational age between 24-34 weeks
- Primary complaints or symptoms indicating threatened preterm delivery
- Intact membranes

Exclusion Criteria

- Triplets or more foetuses
- Contra-indication for tocolysis

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Delivery within 7 days. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Gestational age at delivery, birth weight, neonatal morbidity, neonatal<br /><br>mortality. </p><br>