Registry for operative treatment and outcome of single, multiple and syndromic craniosynostosis

Registry for operative treatment and outcome of single, multiple and syndromic craniosynostosis - Registry for cranioynostosis treatment

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00025162

Enrollment

1000

Registered

2021-06-11

Start date

2021-09-01

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

Q75.0 Q75.1

Interventions

Group 1: all children undergoing operative (individualized) craniosynostosis correction

Eligibility

Sex/Gender

All

Age

No minimum to 40 Years

Inclusion criteria

Inclusion criteria: diagnosed craniosynostosis and performed surgical correction

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

Measure	Time frame
documented morphometric Outcome (3D-Photography, Craniometric Indices) at age 2 - 5 - later if applicable	—

Secondary

Measure	Time frame
1. PROMs (patient reported outcome measures / questionaires) at ages 2 and 5 2. Questionaires (Ages and Stages Questionaire - ASQ and Strenght and Difficulties Questionaire - SDQ) at ages 3-7 3. documented data about treatment (type of operative procedure, transfusion rate, complications…)	—

Countries

Germany

Contacts

Public ContactMatthias Schulz

Pädiatrische Neurochirurgie Charité Universitätsmedizin Berlin

matthias.schulz@charite.de+49 30 450 560092

Outcome results

None listed

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