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Precision and Clinical Evaluation of Full-Arch Implant-Supported Monolithic Zirconia Fixed Prostheses

Precision and Clinical Evaluation of Full-Arch Implant-Supported Monolithic Zirconia Fixed Prostheses

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105172
Enrollment
Unknown
Registered
2025-06-30
Start date
2025-06-30
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Edentulism or terminal dentition

Interventions

Observation group:None

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adult patients aged >= 18 years, with good general health (ASA Physical Status Classification I–II); 2. Patients with edentulous jaws or terminal dentition requiring half-arch or full-arch implant surgery and fixed continuous prosthetic rehabilitation; 3. Sufficient alveolar bone volume for implant placement, as assessed by CBCT (bone height >= 8 mm, bone width >= 5 mm); 4. Willing to undergo implant-supported monolithic zirconia fixed prosthetic treatment; 5. Good patient compliance, with the ability to complete at least one year of follow-up; 6. Generally healthy and clinically assessed as fit for surgery; 7. Voluntary participation with signed informed consent;

Exclusion criteria

Exclusion criteria: 1. Presence of any systemic condition that may contraindicate implant surgery, such as uncontrolled diabetes or hypertension, immunodeficiency, coagulopathy, history of radiotherapy or chemotherapy, alcohol or drug abuse, or current use of oral and/or intravenous bisphosphonates; 2. Poor oral hygiene or inability to maintain oral hygiene according to professional instructions; 3. Heavy smokers (>10 cigarettes/day) or individuals with alcohol dependence; 4. Active oral infections or severe soft and/or hard tissue diseases in the oral cavity; 5. Pregnant or lactating women (women of childbearing potential with high likelihood of pregnancy must undergo pregnancy screening); 6. Patients who are medically unfit or unable to tolerate implant surgery; 7. Individuals with psychiatric disorders or poor compliance who are unable to complete scheduled follow-ups; 8. Any other condition deemed unsuitable for study participation by the investigators;

Design outcomes

Primary

MeasureTime frame
Postoperative complications and adverse outcomes;

Secondary

MeasureTime frame
passive fit of the prosthesis;Patient satisfaction;

Countries

China

Contacts

Public ContactLinhong Wang

Zhejiang Provincial People's Hospital

wanglinhong03@126.com+86 571 8766 6666

Outcome results

None listed

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