Oral Iplanting
Conditions
Interventions
Experimental group:Implant surgical navigation
Sponsors
Peking University Third Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1) Patients with tooth loss that can be repaired by artificial dental implant; 2) Aged 18 to 70 years, male or non-pregnant and non-lactating female; 3) Voluntarily participate in the trial and sign the informed consent; 4) No obvious inflammation or lesion in the oral soft tissues; 5) To accept postoperative visits in accordance with the study plan.
Exclusion criteria
Exclusion criteria: 1) Female patients who plan to give birth within the next 1 year; 2) Patients with poor general and nutritional status; 3) Patients suffering from endocrine metabolic diseases, hematological system diseases and uncontrolled cardiovascular diseases. 4) Suffering from systemic or local bone diseases such as osteomalacia, osteosclerosis, bone tuberculosis, osteitis, bone tumor, etc.; 5) People suffering from systemic immune diseases; 6) Long-term use of special drugs such as hormones and anticoagulants; 7) Pregnant and lactating women; 8) Patients with mental illness, mental disorders and neurological diseases, such as epilepsy; 9) Patients with jaw bone and mucous membrane lesions; 10) Radiotherapy for the head and neck; 11) Patients with Sjogren's syndrome; 12) Patients with uncontrolled periodontal disease or poor oral hygiene; 13) Bad occlusal habits such as grinding teeth at night; 14) Other circumstances that the investigator considers inappropriate to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compliancerate of navigation and positioning;Working stability;Overall safety; | — |
Secondary
| Measure | Time frame |
|---|---|
| Nativation positioning time;Overall operation satisfaction;System Function Evaluation;Adverse event rate; | — |
Countries
China
Contacts
Public ContactXiao Wang
Peking University Third Hosipital
Outcome results
None listed