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Clinical evaluation of 3D printed short titanium implant

Clinical evaluation of 3D printed short titanium implant

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100051292
Enrollment
Unknown
Registered
2021-09-18
Start date
2021-09-30
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

tooth loss

Interventions

Sponsors

Stomatological Hospital of Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. Patients whose mandibular molar extraction sockets are completely healed and are planning to undergo implant restoration; 3. The distance between the alveolar crest in the edentulous area and the upper wall of the inferior alveolar neural canal measured in CBCT is greater than or equal to 8 mm; 4. No history of periodontal disease and good oral hygiene.

Exclusion criteria

Exclusion criteria: 1. Patients with systemic contraindications to implant surgery and severe liver, kidney and heart insufficiency; 2. Smoking more than 10 cigarettes per day; 3. Occlusal deformity or temporomandibular joint disorder; 4. Patients with severe periodontal disease; 5. Suffering from systemic diseases that may affect osseointegration/tissue healing, such as uncontrolled diabetes (fasting blood glucose greater than 11.1mmol/L), systemic or local bone diseases such as osseointegration, osteitis, and bone tumors; 6. Patients with cardiovascular and cerebrovascular diseases who cannot tolerate surgery; 7. Serious blood system diseases, such as leukemia or other bleeding diseases (such as prolonged prothrombin time greater than 6 seconds); 8. Taking drugs that may affect bone metabolism/tissue healing (bisphosphonates or high-dose adrenal corticosteroids); 9. Patients with radiation osteomyelitis; 10. Those with specific allergic constitution; 11. Bruxism patients; 12. Pregnant or lactating women; 13. Unwilling to participate in clinical research or unable to follow up on time; 14. Other circumstances that are judged by the investigator to be unable to participate in the research.

Design outcomes

Primary

MeasureTime frame
Implant Mobility;modified gingival sulcus bleeding index;Peri-implant pocket probing depth;Plaque index;Implant marginal bone changes;

Secondary

MeasureTime frame
Incidence of mechanical complications;

Countries

China

Contacts

Public ContactLi Dehua

Stomatological Hospital of Fourth Military Medical University

lidehua@fmmu.edu.cn+86 29 84776451

Outcome results

None listed

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