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Clinical application of autonomous dental implant robot based on servo function in maxillary sinus lifting

Clinical application of autonomous dental implant robot based on servo function in maxillary sinus lifting

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102038
Enrollment
Unknown
Registered
2025-05-07
Start date
2024-06-20
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Dentition Defect

Interventions

robot group:Under robotic assistance, the socket is prepared step-by-step. The maxillary sinus floor is elevated by the robot using the internal sinus lift module, and finally, the implant is placed w
free hand group:The control group surgeries were performed by experienced surgeon. The procedure required the use of the osteotome technique to remove the sinus floor bone, manually elevate the maxill

Sponsors

School of Stomatology, The Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age >=20 and <=70 years old, regardless of gender; 2. Patients with missing teeth in the maxillary posterior region requiring maxillary sinus floor elevation for implant placement; 3. No soft or hard tissue defects or lesions in the implant area that would affect implant placement; 4. Participants voluntarily agree to participate and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with poor general health or nutritional status; 2. Patients with uncontrolled endocrine or metabolic diseases (e.g., fasting blood glucose >=10 mmol/L); 3. Patients with uncontrolled hematological or cardiovascular diseases; 4. Systemic or local bone diseases considered contraindications for implant restoration, such as bone tuberculosis, osteitis, bone tumors, etc.; 5. Patients with systemic autoimmune diseases or infectious diseases; 6. Individuals on long-term use of specific medications such as hormones, anticoagulants, bisphosphonates, etc.; 7. Pregnant women, women of childbearing age with pregnancy intentions, and lactating women; 8. Patients with neurological disorders, such as epilepsy; 9. Patients with psychiatric disorders or psychological barriers; 10. Individuals with pathological changes in the jawbone; 11. Patients with pathological mucosal lesions; 12. Patients who have undergone head and neck radiotherapy; 13. Patients with Sjögren's syndrome; 14. Individuals with uncontrolled periodontal disease or extremely poor oral hygiene; 15. Individuals with harmful occlusal habits, such as bruxism; 16. Individuals who smoke more than 10 cigarettes per day; 17. Individuals who have participated in other clinical trials within the past three months; 18. Other conditions deemed unsuitable for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
sinus membrane perforation rate;implant placement accuracy;

Secondary

MeasureTime frame
surgical duration;Patient objective evaluation;

Countries

China

Contacts

Public ContactRui Xie

School of Stomatology, The Fourth Military Medical University

ruixie6@foxmail.com+86 181 6197 8067

Outcome results

None listed

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