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Study of the effectiveness of the hydroxyapatite (HA) and b-TCP artificial bone graft material in implant treatment(Randomized controlled trials)

Study of the effectiveness of the hydroxyapatite (HA) and b-TCP artificial bone graft material in implant treatment(Randomized controlled trials) - Study of the effectiveness of the artificial bone graft material

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024036
Enrollment
20
Registered
2016-09-14
Start date
2016-02-02
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

missing teeth

Interventions

Hydroxyapatite group b-TCP group

Sponsors

Kagoshima university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The subjects that there is a defect site of the tooth that requires the implant treatment with a bone augmentation.

Exclusion criteria

Exclusion criteria: Patients with underlying disease can not be performed the implant treatment and excluded.

Design outcomes

Primary

MeasureTime frame
Evaluation of bone augmentation site by CT imaging—

Countries

Japan

Contacts

Public ContactShimotahira naohiro

Kagoshima university Department of oral and maxillofacial prosthodontics

n-shimo@dent.kagoshima-u.ac.jp099-275-6222

Outcome results

None listed

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