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Clinical study on miantainig the natural contours of gingival with fiber splint afer immediate implantation and restoration in aesthetic area

Clinical study on miantainig the natural contours of gingival with fiber splint afer immediate implantation and restoration in aesthetic area

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068934
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

N/A

Interventions

Experimental group:Immediate restoration with fiber splint after immediate implantation at aesthetic area
Control group:Restoration after osseointegration

Sponsors

Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >18 years; 2. Maxillary 3-3 needs to be extracted after trauma; 3. There are 1-2 complete tooth surfaces in the crown of the patient's affected tooth; 4. The affected tooth has proximal and distal adjacent teeth; 5. Opening degree >30mm; 6. Stable occlusion of the proximal and distal teeth of the affected tooth; 7. The immediate initial stability of implant implantation was less than 35N·cm.

Exclusion criteria

Exclusion criteria: 1. Insufficient interalveolar distance for implant placement and repair; 2. Labial plate defect; 3. Untreated severe dental caries or uncontrolled periodontal disease in adjacent teeth; 4. The vertical bone loss of the affected tooth measured from the buccal ridge in the bone of the adjacent tooth exceeds 2mm; 5. Class ? malformations; 6. Smoking or drinking alcohol in the past 6 months; 7. Uncontrolled diabetes; 8. Use any substance that affects bone metabolism; 9. History of radiotherapy to the head and neck; 10. Pregnant patients; 11. Systemic or local diseases or conditions affecting postoperative healing or osseous union; 12. Inability or unwillingness to follow up to 2 years as scheduled.

Design outcomes

Primary

MeasureTime frame
Height of gingival papilla;

Countries

China

Contacts

Public ContactJiang Long

Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine

jianglong25a@163.com+86 138 1656 8151

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 26, 2026