Socket Shield With Immediate Implant Stability

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-04-12

Study Completion Date

2021-02-24

Brief Summary

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To evaluate socket shield technique either placing implant in direct contact to tooth fragment versus gap created between the tooth and implant.

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Detailed Description

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Patients with a non-restorable tooth located in anterior maxillary arch was included in this study, patients were divided into two groups, eight implants per group, both groups had socket shield, group 1 will have implant in direct contact with shield, second group had a gap between dental implant and shield. soft tissue stability, bone width and implant stability was assessed preoperatively, immediate and 6 months postoperative.

Conditions

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Dental Implant

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Socket shield in direct contact with dental implant

eight partially extracted sockets where implant (Neobiotech) was placed in direct contact to socket shield

Group Type ACTIVE_COMPARATOR

Dental implant

Intervention Type DEVICE

Comparative

Socket shield with gap and xenograft with dental implant

eight partially extracted sockets where a gap was left between implant (Neobiotech) and socket shield

Group Type ACTIVE_COMPARATOR

Dental implant

Intervention Type DEVICE

Comparative

Interventions

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Dental implant

Comparative

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients with a non-restorable tooth located in anterior maxillary arch (upper right second premolar to upper left second premolar). Tooth to be extracted is endodontically treated and free from periapical infection.
2. Systemic free patients according to modified Cornell medical index (Brodmank and Erdmann 1949).
3. Patients with good compliance.

Exclusion Criteria

1. Teeth with current acute periapical infection or sinus tracts.
2. Heavy smokers and patients with bruxism habits.
3. Patients with poor oral hygiene or not willing to perform oral hygiene measures.
4. Vulnerable groups (as pregnant females and decisionally impaired individuals).

Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No