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

'easy-graft CRYSTAL' Dental Artificial Bone Power 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
ChiCTR1800016833
Enrollment
Unknown
Registered
2018-06-27
Start date
2017-12-12
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 CRYASTAL
Control:BoneMedik-DM

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;Dental artificial bone powder image analysis;

Countries

China

Contacts

Public ContactXiao Wang

Peking University Third Hospital

bysywangxiao@163.com+86 13601067229

Outcome results

None listed

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