NCT01641523View on ClinicalTrials.gov

Controlled Study in Cranioplasty Reconstruction

CompletedOBSERVATIONAL
Enrollment

91

Participants

Timeline

Start Date

January 31, 2007

Primary Completion Date

January 31, 2007

Study Completion Date

September 30, 2011

Conditions
Cerebral Decompression InjuryCranioplasty
Interventions
DEVICE

CustomBone Service

customized hydroxyapatite cranial prosthesis

All Listed Sponsors
collaborator

Fin-Ceramica Faenza Spa

INDUSTRY

lead

Azienda Ospedaliero-Universitaria di Parma

OTHER

NCT01641523 - Controlled Study in Cranioplasty Reconstruction | Biotech Hunter | Biotech Hunter