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PRETWINSCREEN - A multi-disciplinary approach for a personalized prenatal diagnostics and care for twin pregnancies

PRETWINSCREEN - A multi-disciplinary approach for a personalized prenatal diagnostics and care for twin pregnancies - PRETWINSCREEN

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00023441
Enrollment
1200
Registered
2020-11-02
Start date
2021-04-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

O30.0 O43.0 O36.5 O14.9

Interventions

Group 1: Twin pregnancy Patients with existing twin pregnancies (both monochorial and dichorial) will be included in the study after written consent has been obtained. After recruitment, intensive ca

Sponsors

Abteilung für Geburtshilfe und Pränatale MedizinUniversitätsklinikum Bonn
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Mother's ability to consent - Signed declaration of consent - Presence of a twin pregnancy - gestational age <13+6 weeks at time of inclusion

Exclusion criteria

Exclusion criteria: - death of a twin 2 fetuses) - Indication for termination of pregnancy from maternal indication

Design outcomes

Primary

MeasureTime frame
We aim to develop a multi-marker, personalized, and predictive model for prenatal identification of twin pregnancies that are at risk for developing feto-maternal complications so that better care and preventive measures can be offered.

Secondary

MeasureTime frame
The following complications should be checked and evaluated by the register: - Proportion of study participants with one of the following complications: o Preeclampsia (PE) o Gestational diabetes (GDM, dietary adjusted or insulin required) o Feto-fetal transfusion syndrome (TTTS, twin-to-twin transfusion syndrome) o Selective intrauterine growth restriction (sIUGR, selective intrauterine growth restriction) - Causes of death intrauterine - Proportion of study participants with necessary intervention during pregnancy due to one of the above mentioned complications: o Intrauterine laser therapy with TTTS o Cord-clamping at sIUGR o Amniotic drainage o Invasive prenatal diagnostics (AC, CVS) for fetal chromosomal abnormalities o Antihypertensive or anticonvulsive therapy for PE o Insulin therapy for insulin-dependent GDM - Birth / Premature birth o Average age at birth o Birth weight (Z-scores; percentiles) or weight difference between fat 1 and 2 o Maternal morbidity / mortality o Childhood morbidity / mortality - Number of AEs / adverse outcomes (prenatal, postnatal) - maternal and infantile - Average number of days of maternal and neonatal hospitalization due to complications

Countries

Canada, Germany, Israel, Spain, United Kingdom

Contacts

Public ContactAnnegret Geipel

Abteilung für Geburtshilfe und Pränatale MedizinUniversitätsklinikum Bonn

annegret.geipel@ukbonn.de+49-228-287 37116

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026