Skip to content

Accuracy of Semi-Autonomous Robot-Assisted Implant Placement in Edentulous and Terminal Dentition Patients: A Prospective Single-Arm Observational Study

Accuracy of Semi-Autonomous Robot-Assisted Implant Placement in Edentulous and Terminal Dentition Patients: A Prospective Single-Arm Observational Study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116260
Enrollment
Unknown
Registered
2026-01-07
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Presence of dentition defects (complete edentulism) or terminal dentition

Interventions

Semi-autonomous robotic group:None

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 and 80 years; 2.Patients with dentition defects (complete edentulism) or terminal dentition in the maxilla and/or mandible who are scheduled to receive implant-supported rehabilitation. 3.No severe soft or hard tissue defects or other pathological conditions in the implant site that would compromise the feasibility of implant surgery. 4.Voluntary participation in this study with signed informed consent, and willingness to comply with preoperative and postoperative imaging examinations as well as short-term postoperative follow-up.

Exclusion criteria

Exclusion criteria: 1.History of maxillofacial radiotherapy, or previous treatment with bisphosphonates or denosumab. 2.History of myocardial infarction within the past 6 months. 3.Inability to maintain adequate oral hygiene despite standardized oral hygiene instruction. 4.Severe bone defects in the planned implant site that preclude conventional implant rehabilitation. 5.Failure to provide written informed consent. 6.Inability to comply with preoperative and postoperative imaging examinations or short-term postoperative follow-up.

Design outcomes

Primary

MeasureTime frame
Angular deviation;

Secondary

MeasureTime frame
Apical lateral deviation;Apical global deviation;Apical depth deviation;Platform depth deviation;Platform global deviation;Platform lateral deviation;

Countries

China

Contacts

Public ContactYude Ding

Zhejiang Provincial People's Hospital

392981446@qq.com+86 571 8589 3206

Outcome results

None listed

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