UnknownNot Applicable

Clinical Study of FRC Implant to Treat Skull Bone Defects

Finland19 participantsStarted 2013-01

Plain-language summary

Bioactive fibre-reinforced composite implant is used for reconstruction of skull bone defects and orbital floor defects. Functional and aesthetic outcome is assessed by patient and doctor.

Who can participate

SexALL

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Inclusion Criteria: Study arm 1: * patients with skull bone defect * reconstruction indications fullfilled Study arm 2: * patients with orbital floor defect * reconstruction indication fullfilled Exclusion Criteria: * if informed consent cannot be obtained

What they're measuring

Functional outcome (a composition of following measures)

Timeframe: 2 year follow-up

Trial details

NCT IDNCT01874613

SponsorTurku University Hospital

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2016-12

View on ClinicalTrials.gov More Cranial Bone Defect trials