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Immediate Implant Placement With Connective Tissue Graft or Socket Shield

Immediate Implant Placement Without Connective Tissue Graft or Socket Shield: a Randomized Controlled Clincial Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03594019
Enrollment
40
Registered
2018-07-20
Start date
2019-02-01
Completion date
2022-02-01
Last updated
2019-05-16

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

Conditions

Tooth Fractures

Keywords

immediate implant placement, connective tissue graft, samll dehiscence

Brief summary

The present study aims to evaluate the clinical outcomes of immediate implant placement with connective tissue graft or socket shield. Previous studies have demonstrate the intact buccal bone plate plays an important role in the stability of peri-implant soft tissue around immediately placed implants. However, it remains controverisal whether soft tissue stability could be achieved in immediate implant placement with connective tissue graft or socket shield.

Interventions

PROCEDUREConnective tissue graft

Connective tissue graft (CTG) is an oral and maxillofacial surgical procedure first described by Alan Edel in 1974. It includes the preparation the recipient site of tissue exhibiting recession by incising the gingival, obtaining the CTG from the donor site, securing the CTG at the recipient site and suturing the incised gingival tissue at both the donor and recipient sites.

The procedure is used to split the teeth and preserve the buccal part

PROCEDUREImmediate implant placement

The implant will be placed in the frest socket immediately after tooth extraction

Sponsors

Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients in need of single implant treatment in anterior maxilla Patients with small dehiscence in the buccal bone plate (\<2mm vertical bone loss and \<5mm horizontal bone loss) Patients with natural teeth adjacent to implant site

Exclusion criteria

* Uncontrolled periodontal diseases Heavy smokers (\>10 cigarettes/day) Unwilling to participate in the present study

Design outcomes

Primary

MeasureTime frameDescription
pink esthetic score (PES)1 yearAn objective index introduced by Furhauser et al. 2005

Secondary

MeasureTime frameDescription
mucosal recession1 yearthe mid-buccal mucosal level change from baseline to follow-up
marginal bone loss1 yearthe mesial and dital marginal bone loss from baseline to follow-up evaluated by peri-apical X-ray.
pocket probing depth1 yearthe pocket depth at six sites around implant will be detected by periodontal probe
bleeding on probing1 yearthe percentage of bleeding after probing by periodontal probe

Countries

China

Contacts

Primary ContactJunyu Shi, PhD
sakyamuni_jin@163.com081 53315299

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026