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Clinical Trials in the USA / NCT06762691
Starting soon Observational

Cranial Remolding Orthosis Registry

NCT06762691 · tracked via the Priya Life Science USA tracker
Sponsor
Otto Bock HealthCare LP
Phase
Observational
Started
2025-04
Last updated
2025-01-07

Condition(s) studied

PlagiocephalyBrachycephalyAsymmetric Head

Investigational drug(s) / intervention(s)

MyCRO BandTraditional CRO

MyCRO Band: A 3D-printed cranial remolding orthosis

Traditional CRO: A traditionally manufactured cranial remolding orthosis such as the Orthomerica Starband

Study summary

A registry of infants fitted with a cranial remolding orthosis.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient has been evaluated and successfully scanned for a MyCRO Band or similar CRO * Patient's parent(s) or legal guardian(s) are able to communicate, provide feedback, understand and follow instructions during the course of the registry. * Parent(s) or legal guardian(s) are willing to provide informed consent. Exclusion Criteria: * Patient is geographically inaccessible to comply and participate in the registry.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Wright & Filippis Madison Heights Michigan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06762691 on ClinicalTrials.gov ↗ ← All trials in the USA