ational postpartum psychosis prevention study

Completed

• Conditions: 10036411; 10026753; puerperal psychosis; postpartum psychosis

• Registration Number: NL-OMON47010
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 310

Inclusion Criteria

- Age > 18 years
- A history of bipolar disorder and/or postpartum psychosis
- Women who are able to complete Dutch questionnaires;Offspring: between 2 and 5 years of age

Exclusion Criteria

None.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Primary outcome will be peripartum relapse (during pregnancy or within 3 months<br /><br>postpartum): any episode fulfilling DSM-IV criteria for<br /><br>mania/depression/psychosis or any other episode, severe enough to warrant<br /><br>treatment.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Obstetric complications, neonatal adverse outcome, infant neurodevelopment.<br /><br>Blood cells and serum biomarkers predictive for relapse.</p><br>