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Placenta perfusion and sufficiency study

Placenta perfusion and sufficiency study - P2S-study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON53343
Enrollment
10
Registered
2023-05-02
Start date
2023-08-11
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

placenta dysfunction placenta insufficiency

Interventions

None listed

Sponsors

Maxima Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Age 18 years or higher - Between 14-16 weeks gestation - Placenta anterior - BMI

Exclusion criteria

Exclusion criteria: - Non-intact pregnancy - Vanishing twin - Multiple gestations - Congenital or anatomical anomalies

Design outcomes

Primary

MeasureTime frame
The assessment of the reproducibility of measuring the placental perfusion in women with singleton pregnancies between 14- and 16-weeks*gestational age

Secondary

MeasureTime frame
1. To assess whether it is possible to repeatedly measure the blood velocity and diameter of the uterine arteries and veins, and umbilical arteries and vein. 2. What are the differences in measurements between the two umbilical arteries? 3. Does a relation between the uterine artery and vein flow exist? 4. Does a relation between the umbilical arteries and vein flow exist? 5. The assessment of intra-observer variability.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)