National postpartum psychosis prevention study

National postpartum psychosis prevention study - NP3-Study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON47010

Enrollment

310

Registered

2013-11-19

Start date

2013-12-02

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

"puerperal psychosis" postpartum psychosis

Interventions

None listed

Eligibility

Age

2 Years to 99 Years

Inclusion criteria

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

Exclusion criteria: None.

Design outcomes

Secondary

Measure	Time frame
Obstetric complications, neonatal adverse outcome, infant neurodevelopment. Blood cells and serum biomarkers predictive for relapse.	—

Primary

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

Countries

Netherlands

Outcome results