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Intraoperative real-time intraoral scanning for accuracy and clinical efficacy of immediate single-tooth implant restoration in the posterior region

Intraoperative real-time intraoral scanning for accuracy and clinical efficacy of immediate single-tooth implant restoration in the posterior region

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111985
Enrollment
Unknown
Registered
2025-11-08
Start date
2025-06-11
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Dental defect

Interventions

Experiment (Immediate IOS):The patient will undergo the second-stage surgery in 3 months and wear the final prosthesis (T1) simultaneously
Control (Regular IOS):Three months after the implant placement surgery (T0), the subjects underwent a second-stage surgery for intraoral scanning to obtain digital impressi

Sponsors

Stomatology Hospital,Zhejiang University School Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Be over 18 years old; 2. No obvious pharyngeal reflex, oropharyngeal diseases, etc; 3. In the posterior region, there is a single missing tooth, with natural teeth present on both sides and in occlusion. The occlusal space and mesial-distal space are sufficient, and the adjacent teeth are not tilted. It is suitable for implant placement, or after appropriate adjustments, it meets the indications for implant surgery; 4. The patient is able to cooperate with treatment; 5. The oral hygiene is good, with BOP less than 20% and probing depth less than 5mm.

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrolled systemic diseases, such as uncontrolled severe diabetes, heart disease, hypertension, etc. 2. Patients who smoke more than 10 cigarettes per day; 3. Patients with uncontrolled periodontitis; 4. Patients with tumors or other severe chronic diseases in the implant area; 5. Patients with acute infection in the implant area; 6. Pregnant, gestational, or lactating women; 7. Patients with severe oropharyngeal nausea, limited mouth opening, temporomandibular joint disorder, and other issues that prevent them from cooperating with treatment; 8. Patients undergoing replantation and bone augmentation surgery, as well as other patients deemed unsuitable for participation in this study by the researchers.

Design outcomes

Primary

MeasureTime frame
Crown accuracy assessment;

Secondary

MeasureTime frame
Gingival biological indicators;Assessment of working time beside the chair;Evaluation of repair effect;

Countries

China

Contacts

Public ContactFuming He

The Affiliated Stomatological Hospital of Zhejiang University School of Medicine

hfm@zju.edu.cn+86 13516817697

Outcome results

None listed

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