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Bioactive Glass Composite Implants in Cranial Bone Reconstruction

NCT01202838 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2010-09-16

No results posted yet for this study

Summary

The purpose of this study is to study composites of bioactive glass and methylmetacrylate with glass fibre reinforcement in cranial bone defect reconstruction.

Conditions

  • Bone Substitutes

Interventions

DEVICE

Composite Implant

Subjects receiving composite implants

Sponsors & Collaborators

  • Turku University Hospital

    lead OTHER_GOV

  • University of Turku

    collaborator OTHER

Principal Investigators

  • Matti J Peltola, MD, PhD, DDS · Turku University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2012-12-31
Completion
2012-12-31

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01202838 on ClinicalTrials.gov