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Fetotoxicity of NSAIDS and RAAS-inhibitors in the 2nd and 3rd trimester of pregnancy (paediatric-nephrologic approach)

Conditions
I10
Q61.4
Q60
Essential (primary) hypertension
Renal dysplasia
Renal 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
NameTimeMethod
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
NameTimeMethod
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.
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