malfunctioning placenta Uteroplacental insufficiency
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Groningen
Eligibility
Inclusion criteria
Inclusion criteria: Singleton pregnant women referred for a routine 13-week scan to the UMCG in the context of a cT and/or indicated screening anomaly scan will be included.
Exclusion criteria
Exclusion criteria: Age
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in Doppler US parameters measured during the 13-week scan in the uteroplacental insufficiency (UPI) population and the non-UPI population. | — |
Secondary
| Measure | Time frame |
|---|---|
| Biomarker analyzes in 13-week blood samples between pregnancies complicated by UPI and non-UPI. | — |
Countries
Netherlands
Outcome results
None listed