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The effect of customized zirconia abutment on biological attachment

The effect of customized zirconia abutment on biological attachment

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037689
Enrollment
Unknown
Registered
2020-08-30
Start date
2020-08-17
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

defect of dentition

Interventions

Pure titanium:Pure titanium
Titanium base 1mm:Titanium base 1mm
Titanium base 2mm:Titanium base 2mm
Titanium base 3mm:Titanium base 3mm

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with missing upper/mandibular molars planned for implant restoration; 2. Patients with good bone condition and no need for bone graft surgery ; 3. The width of the buccal-lingual keratinized mucosa is greater than 8mm; 4. The initial stability of the implant is greater than/equal to 30Ncm and does not need to be implanted for healing; 5. The thickness of the mucosa in the operation area is greater than/equal to 3mm;(6)Missing teeth for at least 6 months; 7. ASA I~II classification of American Society of Anesthesiologists; 8. Aged over 18 years; 9. Good oral hygiene and good compliance.

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrolled periodontitis in their remaining teeth; 2. Smoking patients; 3. Patients with uncontrolled infection in the operation area and the whole body; 4. Patients with systemic diseases: Patients with uncontrolled diabetes, cardiovascular diseases, immune system diseases, coagulation disorders and other blood diseases and severe osteoporosis; 5. Patients with long-term medication, especially those with history of steroids, antiepileptic drugs and bisphosphonates; 6. Patients with special infection: HIV, hepatitis B, syphilis infection, etc.; 7. Bruxism patients; 8. The subjects who did not agree to participate in the experiment did not sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Mucosal tissue section around implant;Implant clinical examination;

Secondary

MeasureTime frame
The thickness of the mucosa (the crest).;

Countries

China

Contacts

Public ContactJingwen Yang

Peking University stomatological hospital

jingwen.yang@foxmail.com+86 15101157982

Outcome results

None listed

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