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Magnetic Resonance Imaging in patients with craniosynostosis.

Magnetic Resonance Imaging in patients with craniosynostosis. - MRI in craniosynostosis

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38890
Enrollment
80
Registered
2013-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

ontwikkeling van hersenen (in relatie tot het te vroeg sluiten van schedelnaden) Craniosynostosis premature fusion of the skullsutures

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

Inclusion criteria

Inclusion criteria: Patients with one of the following diagnoses: - Complex craniosynostosis - Syndromic craniosynostosis - Trigonocephaly - Scaphocephaly And: - Between 0 and 2 years of age

Exclusion criteria

Exclusion criteria: Patients with any metallic object in their skull. Patients with a known allergy to the used anaesthetic agent.

Design outcomes

Primary

MeasureTime frame
The main study parameters follow from the MR scan outcomes. The cerebral blood flow will be measured in ml/g/min per region of the brain. DTI data is expressed in fractional anisotropy (FA) and Apparent Diffusion Coefficient (ADC) values for all regions of interest. The endpoint for the individual patient is reached after the last MR scan is made. Standard clinical follow-up will last until the patient is 18 years of age.

Secondary

MeasureTime frame
primary study parameters will be correlated to the outcome of neuro-cognitive test performed during standard clinical follow-up.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)