Fetotoxicity of NSAIDS and RAAS-inhibitors in the 2nd and 3rd trimester of pregnancy (paediatric-nephrologic approach)
- Conditions
- I10Q61.4Q60Essential (primary) hypertensionRenal dysplasiaRenal agenesis and other reduction defects of kidney
- Registration Number
- DRKS00011861
- Lead Sponsor
- Pharmakovigilanzzentrum Embryonaltoxikologie Charité-Universitätsmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 287
Inclusion Criteria
Patients who had an apointment in the pediatric clinic for nephrology in the years 2015 and 2016.
Exclusion Criteria
none
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Are renal hypoplasia or renal dysplasia or hypertension in children and adolescents more frequent when the mother has taken an NSAID, metamizole or RAAS-inhibitor in the second half of pregnancy? For this purpose, all patients who were seen in the Charité clinic for pediatric nephrology in the past two years will be contacted by questionnaire.
- Secondary Outcome Measures
Name Time Method Are there any signs of a minimum exposure time and/or a minimum dose? For this purpose, all patients who were seen in the Charité clinic for pediatric nephrology in the past two years will be contacted by questionnaire.