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Clinical Trials/NCT05658419
NCT05658419
Completed
Not Applicable

Evaluation of Immediate Loaded Implants Placed Using the Socket Shield Technique in the Esthetic Zone

Alexandria University1 site in 1 country20 target enrollmentJanuary 14, 2021
ConditionsBone Loss

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bone Loss
Sponsor
Alexandria University
Enrollment
20
Locations
1
Primary Endpoint
radiographic bone level
Status
Completed
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 14, 2021
End Date
August 5, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

radiographic bone level

Time Frame: 6 months

vertical and horizontal bone loss

Study Sites (1)

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