Skip to content

Clinical Trial on PREnatal Dexamethasone In Congenital adrenal hyperplasia Therapy - PREDICT -

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511702-23-00
Acronym
KKS-292
Enrollment
122
Registered
2024-11-19
Start date
2025-08-05
Completion date
Unknown
Last updated
2025-12-02

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

Conditions

Congenital adrenal hyperplasia

Brief summary

Closure of urogenital sinus (Prader stage), Gestational weight gain (GWG) of mother

Detailed description

Parameters of treatment consequences/safety in treated mothers and children, safety parameters: stillbirths, miscarriages, maternal side effects and adverse events, serious adverse events (AEs, SAEs) in treated mothers and children, maternal quality of life, maternal mental health and sleep, child´s birth weight and height at birth, week of gestation at birth, infant nervous system development, malformations in the child)

Interventions

DRUGDexamethason 0.21mg
DRUGDexamethason 0.15mg
DRUGDexamethason 0.41mg
DRUGDexamethason 0.5mg

Sponsors

Philipps-Universitaet Marburg
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Closure of urogenital sinus (Prader stage), Gestational weight gain (GWG) of mother

Secondary

MeasureTime frame
Parameters of treatment consequences/safety in treated mothers and children, safety parameters: stillbirths, miscarriages, maternal side effects and adverse events, serious adverse events (AEs, SAEs) in treated mothers and children, maternal quality of life, maternal mental health and sleep, child´s birth weight and height at birth, week of gestation at birth, infant nervous system development, malformations in the child)

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026