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'easy-graft CLASSIC' Dental Artificial Bone Powder for Damage Restoration of Non-immediately Load-bearing Parts of Jaw Bone

'easy-graft CLASSIC' Dental Artificial Bone Powder for Damage Restoration of Non-immediately Load-bearing Parts of Jaw Bone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016835
Enrollment
Unknown
Registered
2018-06-27
Start date
2017-02-09
Completion date
Unknown
Last updated
2018-07-02

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

Conditions

Damage Restoration of Non-immediately Load-bearing Parts of Jaw Bone

Interventions

Test:easy-graft CLASSIC
Control :Cerasorb M

Sponsors

Peking University School of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18-60 years old male and female; 2) Persons whose tooth needs to be extracted; 3) Local wound can be sutured tightly by surgery; 4) Subjects are willing to participate in the trial and sign the informed consent document.

Exclusion criteria

Exclusion criteria: 1) Pregnant or lactating women; 2) Patients with infectious disease; 3) Patients with severe systemic disease; 4) Subjects with severe allergic constitution; 5) Patients with severe vessel or nervous system disease; 6) Patients with severe degenerative disease; 7) Patients who cannot coordinate with medical treatment, including the persons who dont follow postoperative guidance and abuse drugs and alcohol; 8) Patients with abnormal hypercalcemia or calcium metabolism; 9) Patients with osteitis diseases like osteomyelitis; 10) Patients with malignant tumor or patients whose local tumor are not removed completely; 11) Patients with severe renal failure; 12) Patients with local infectious parts; 13) Patients who cannot bear bone graft surgery due to general physical conditions (e.g. severe cardiovascular disease, diabetes mellitus and liver and kidney function deficiency)? 14) Subjects who are participating in other medical device trial or drug clinical trial; 15) Patients who have taken anticoagulant drugs or have surgical contraindication in recent week; 16) Subjects who are not suitable to participate in the clinical trial in researchers opinion

Design outcomes

Primary

MeasureTime frame
Newborn bone volume fraction BV/TV;

Secondary

MeasureTime frame
Alveolar bone height changes ?H;artificial bone powder image;

Countries

China

Contacts

Public ContactXiao Wang

Peking University School of Stomatology

bysywangxiao@163.com+86 13601067229

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026