Asssessment of bioabsorbable hydroxyapatite for craniofacial surgery

Asssessment of bioabsorbable hydroxyapatite for craniofacial surgery - Asssessment of bioabsorbable hydroxyapatite

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000024125

Enrollment

Registered

2016-09-21

Start date

2015-08-06

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

Bone defect at craniofacial region

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Alveolar cleft, the patient performed cranioplasty for the defect of the cranium

Exclusion criteria

Exclusion criteria: THe patients of osteogenesis dysostosis, or chromosome aberration.

Design outcomes

Primary

Measure	Time frame
The bone volume 1 year after the operation	—

Secondary

Measure	Time frame
The number of patient-controlled intravenous analgesia use	—

Countries

Japan

Contacts

Public ContactYoshiaki Sakamoto

Keio University School of Medicine Department of Plastic and Reconstructive Surgery

ysakamoto@z8.keio.jp0353633814

Outcome results