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The clinical application of dental implant robotic system in full-arch implant patients :a clinical trial

The clinical application of dental implant robotic system in full-arch implant patients :a clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073761
Enrollment
Unknown
Registered
2023-07-20
Start date
2022-05-07
Completion date
Unknown
Last updated
2023-07-30

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

Conditions

fully edentulous jaw

Interventions

Experimental group:Osteotomies and implant placement in fully edentulous patients will be performed by using dental implant robotic system

Sponsors

the School of Stomatology, The Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age =18 and =70, no gender limitation; 2. fully edentulous jaw patients or terminal dentition with the need for implants; 3. No soft and hard tissue defects or lesions affecting implant implantation were found in implant implantation area; 4. Subjects voluntarily participate and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Poor general condition and nutritional status; 2. Patients with uncontrolled endocrine and metabolic diseases (e.g., fasting blood glucose =10mmol/L); 3. Patients with blood system diseases and uncontrolled cardiovascular diseases; 4. Systemic or local bone diseases are considered contraindications for implant repair, such as bone tuberculosis, osteitis, bone tumor, etc. 5. Patients with systemic immune diseases and infectious diseases; 6. Long-term use of special drugs such as hormones, anticoagulants, bisphosphonates, etc. 7. Pregnant and intended pregnant women of childbearing age and breastfeeding women; 8. Neurological diseases, such as epilepsy; 9. People with mental illness or mental disorder; 10. Pathological changes of jaw bone; 11. Pathological mucosal lesions; 12. Patients after radiotherapy for head and neck; 13. Sjogren's Syndrome; 14. Uncontrolled periodontal disease or poor oral hygiene; 15. Bad occlusal habit, bruxism, etc. 16. Smokers who smoke more than 10 cigarettes/day; 17. Participants in other clinical trials in the last three months; 18. Other conditions that the investigator considers inappropriate for participation in the trial.

Design outcomes

Primary

MeasureTime frame
the accuracy of implant;surgery duration;

Secondary

MeasureTime frame
postoperative questionnaire survey;Intraoperative Complications;primary stability;periodontal status;

Countries

China

Contacts

Public ContactBai Shizhu

the School of Stomatology, The Fourth Military Medical University

baishizhu@foxmail.com+86 29 8477 4511

Outcome results

None listed

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