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Bone augmentation with tissue engineered bone

Bone augmentation with tissue engineered bone - Bone augmentation with tissue engineered bone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006720
Enrollment
100
Registered
2011-11-14
Start date
2001-11-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Atrophy of alveolar bone

Interventions

Transplantation of tissue engineered bone

Sponsors

Department of Oral and Maxillofacial Surgery, Nagoya University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patients who desire to undergo bone regeneration and agree with this treatment.

Exclusion criteria

Exclusion criteria: Patient who have severe complications, infectious disease, or other special conditions that is not appropriate to undergo this study.

Design outcomes

Primary

MeasureTime frame
The evaluation of safety and clinical efficacy of tissue engineered bone

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026