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A Clinical Trial on the Effects of Immediate Implant Placement with Socket Shield Technique in Esthetic Region on Peri-implant Soft and Hard Tissue

A Clinical Trial on the Effects of Immediate Implant Placement with Socket Shield Technique in Esthetic Region on Peri-implant Soft and Hard Tissue

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119635
Enrollment
Unknown
Registered
2026-03-02
Start date
2026-03-09
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Partial edentulism

Interventions

Socket Shield Technique:After tooth decoronation, the remaining root was reduced to approximately 1 mm above the alveolar crest using a diamond bur. The planned implant position was marked within the
Immediate Implant Placement:A minimally invasive, flapless tooth extraction was performed. The extraction socket was thoroughly debrided and irrigated with sterile saline. The integrity of the buccal

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Patients requiring implant-supported restoration because maxillary anterior tooth/teeth cannot be preserved due to trauma or endodontic/pulpal disease. 2.Patients aged 18 years or older. 3.Intact buccal/ labial bone plate. 4.The root is positioned within the alveolar bone and the site is suitable for immediate implant placement. 5.The tooth planned for extraction has no deep periodontal pocket > 3 mm and no periapical lesion larger than 1 cm in diameter. 6.The patient has full decision-making capacity, can understand and comply with the surgical procedure, and provides written informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with unfavorable occlusal conditions for immediate implant placement, such as deep overbite. 2.Patients with poor periodontal conditions or whose periodontal status cannot be controlled after treatment. 3.Patients with systemic or local diseases that may impair postoperative healing or osseointegration. 4.Poor treatment compliance.

Design outcomes

Primary

MeasureTime frame
Change in the height of the buccal (labial) bone plate;S;

Secondary

MeasureTime frame
Change in the thickness of the buccal (labial) bone plate;Height and thickness of the buccal (labial) soft tissue;Success rate of implant;Pink esthetic score, PES;

Countries

China

Contacts

Public ContactHuajie Yu

Peking University School and Hospital of Stomatology

yuhuajie666@aliyun.com+86 138 1121 2558

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026