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Clinical evaluation of chairside CAD/CAM integrated fiber-reinforced composite post-and-core

Clinical evaluation of chairside CAD/CAM integrated fiber-reinforced composite post-and-core

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061273
Enrollment
Unknown
Registered
2022-06-18
Start date
2022-06-06
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

tooth defect

Interventions

experimental group:chairside CAD/CAM integrated fiber-reinforced composite post-and-core restoration
control group:metal post-and-core restoration

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patient inclusion criteria: (1) Willing to accept new post and core repair methods; (2) Willing and able to regularly review and follow-up; (3) Receive complete root canal treatment in the dental endodontics specialty; 2. Inclusion criteria for affected teeth: (1) The affected tooth is a single canal anterior tooth; (2) The tooth defect cannot be located under the gingiva, or the defect can be aligned with the gingiva or located on the gingiva after crown lengthening; (3) The root canal treatment has been completed for 2 weeks, and the root canal has no significant curvature, no symptoms such as pain and swelling, and no low-density imaging manifestations on X-ray films; (4) Sufficient root length to ensure that the pile crown ratio is at least 1:1, and the root tip is closed at least 3 mm; (5) There is no untreated periodontitis and looseness exceeding physiological mobility, alveolar bone resorption is limited to 1/3 of the root length, and the tooth is not an isolated tooth or an abutment tooth of FPD or RPD.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Severe systemic diseases; 3. Acute inflammation and tumor of oral cavity and maxillofacial region; 4. Severe or progressive periodontal inflammation; 5. Internal and external absorption of the tooth root.

Design outcomes

Primary

MeasureTime frame
Clinical evaluation;Imaging evaluation;

Secondary

MeasureTime frame
Patient subjective evaluation;

Countries

China

Contacts

Public ContactDeng Xuliang

Peking University School and Hospital of Stomatology

kqdengxuliang@bjmu.edu.cn+86 13501030929

Outcome results

None listed

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