Adherence of antidepressants during pregnancy - naadje
- Conditions
- Pregnant women with psychiatric morbidity and an strong indication for using antidepressants
- Registration Number
- EUCTR2009-011893-13-NL
- Lead Sponsor
- Isala Klinieken
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- Female
- Target Recruitment
- 0
Inclusion Criteria
Patients will be included if they are pregnant, use antidepressants, regardless pharmacological class, and signed informed consent.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Incapacity to follow the study protocol according to the attending specialist.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method