Facially Driven, Fully Digital Full-Mouth Rehabilitation with Guided Implant Placement, TAD-Assisted Molar Intrusion, and Restorative Crowns/Veneers
Facially Driven, Fully Digital Full-Mouth Rehabilitation with Guided Implant Placement, TAD-Assisted Molar Intrusion, and Restorative Crowns/Veneers: Participants will receive full-mouth dental rehabilitation using advanced digital planning. Scans of the teeth, face, and jaw will guide treatment, which may include tooth movement with temporary devices, guided implant placement, and placement of custom veneers and crowns. This approach aims to restore bite function, improve smile esthetics, and ensure accurate, comfortable, and durable results.
Study summary
Participants with bite difficulties, smile dissatisfaction, and missing mandibular molars was rehabilitated using a fully digital, facially driven workflow. Integration of intraoral, facial, and CBCT data guided esthetic design, occlusion, and implant planning, resulting in precise alignment, functional occlusion, and esthetic restoration with veneers, zirconia crowns, TAD-assisted molar intrusion, and guided implants.
Eligibility
Sex
ALL
Min age
20 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria:
* Adults aged 20-45 years with partial or complete edentulism requiring full-mouth rehabilitation.
* Patients with bite dysfunction, malocclusion, or esthetic concerns suitable for digital workflow treatment.
* Adequate bone volume for implant placement or candidates for TAD-assisted tooth movement.
* Willingness to undergo treatment using a fully digital, facially guided workflow and comply with follow-up visits.
* Ability to provide informed consent.
Exclusion Criteria:
* Systemic conditions contraindicating implant or surgical procedures (e.g., uncontrolled diabetes, immunosuppression).
* Active oral infections or untreated periodontal disease.
* Heavy smokers (\>10 cigarettes/day) or substance abuse.
* History of head and neck radiation therapy or bisphosphonate use.
* Pregnancy or breastfeeding.
* Inability to comply with treatment or follow-up protocol.
Primary outcome measure(s)
Implant Stability — 12 months post-treatment Clinical assessment: Absence of implant mobility assessed manually and using opposing instrument pressure.
Radiographic assessment: Periapical radiographs using the paralleling technique to evaluate peri-implant bone levels.
Success criteria: No progressive peri-implant radiolucency and marginal bone loss ≤ 1.5 mm during the first year, in accordance with Albrektsson et al. success criteria.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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