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Accuracy and Clinical Efficacy of a Healing Abutment-Based Intraoral Scanning Occlusal Registration Device inDistal Extension Implant Restorations

Accuracy and Clinical Efficacy of a Healing Abutment-Based Intraoral Scanning Occlusal Registration Device inDistal Extension Implant Restorations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107610
Enrollment
Unknown
Registered
2025-08-14
Start date
2025-08-15
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Partial edentulism

Interventions

Test Group (occlusal registration auxillary):Place the Occlusal Registration auxillary
Control Group (Highest-Profile Healing Abutment):Place the Occlusal Registration auxillary

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1: Age = 20 years and <= 70 years 2: Partial edentulism involving = 2 consecutive posterior teeth with a free-end saddle (Kennedy Class I or II) 3: No significant occlusal abnormalities in the remaining dentition (e.g., premature contact, occlusal interference) and absence of clinical symptoms prior to restoration 4: Periodontal health or completion of comprehensive systematic periodontal therapy 5: Patient has undergone implant surgery and provided signed informed consent 6: Absence of any local or systemic diseases contraindicating implant surgery

Exclusion criteria

Exclusion criteria: 1: Non-free-end partial edentulism 2: Complete edentulism or absence of stable occlusal contacts in the remaining dentition of partially edentulous patients 3: Temporomandibular joint disorders 4: Presence of oral parafunctional habits 5: Pregnancy or lactation 6: Smoking > 10 cigarettes per day 7: Use of corticosteroids or bisphosphonates 8: Physical disabilities or mental illnesses affecting oral hygiene maintenance 9: History of chemotherapy within 5 years prior to surgery or radiotherapy in the head and neck region 10: Any condition potentially compromising study completion or confounding the analysis (e.g., non-compliance, concealed medical history)

Design outcomes

Primary

MeasureTime frame
Occlusal Adjustment Volume;Incidence of Lateral Occlusal Interferences;T-Scan Occlusal Analysis;

Secondary

MeasureTime frame
Articulating Paper Evaluation;Occlusal Adjustment Time;Clinician/Patient Satisfaction;

Countries

China

Contacts

Public ContactQian Ding

Peking University School and Hospital of Stomatology

dingqian.623@163.com+86 151 2003 3697

Outcome results

None listed

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