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Immediate Implant vs.Socket Shield Technique in Esthetic Zone

Not Applicable
Completed
Conditions
Bone Loss
Interventions
Procedure: socket sheild
Registration Number
NCT05658419
Lead Sponsor
Alexandria University
Brief Summary

immediate implant placement versus socket shield approach

Detailed Description

This study was a randomized controlled clinical trial; patients were randomly allocated to two groups: the study group: ten dental implants were placed in the maxillary esthetic zone, implants were placed using the socket shield technique with immediate loading; and the control group: ten implants were placed immediately with immediate loading. Preoperative and 6 months postoperative CBCT were performed for both groups to assess the dimensional changes in the labial bone plates. Implant stability quotients (ISQs), pink esthetic scores and attachment loss were measured at the time of implant placement and 6 months postoperatively.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria

Patients of 20-45 years of both sexes. Good oral hygiene Demonstrating non-restorable maxillary anterior single rooted teeth in the esthetic zone with as far diagnosable.

Fairly intact buccal periodontal tissues. Patients' acceptance to sign the informed consent. Labial bone plates less than 1.5 mm in thickness or cases with labial root curvatures.

Intact root with no mobility in the tooth and no sub-gingival caries.

Exclusion Criteria

Patients with systemic diseases that would interfere with the normal healing such as uncontrolled diabetes mellitus.

History of radiation therapy to the head and neck. No history of bruxism/ para-functional habits. (119) Teeth with periodontal disease, vertical root fracture, horizontal fracture at or below the bone level, and teeth with local pathologic incidents that affect the labial part of the root as external or internal root resorption were also excluded.

Maxillary 1st and 2nd premolars. Pregnant and lactating females.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
control groupsocket sheildimmediate implant placement
study groupsocket sheildsocket shield immediate implant placement
Primary Outcome Measures
NameTimeMethod
radiographic bone level6 months

vertical and horizontal bone loss

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mohamed Mohamed Shehata Elsayed

🇪🇬

Alexandria, Egypt

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