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Clinical Trials/NCT05409950
NCT05409950
Completed
Not Applicable

Evaluation of Socket Shield Technique With Immediate Implant Placement in the Esthetic Zone

Egyptian Russian University1 site in 1 country20 target enrollmentSeptember 16, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alveolar Bone Resorption
Sponsor
Egyptian Russian University
Enrollment
20
Locations
1
Primary Endpoint
Vertical bone loss
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The study was conducted on 20 immediate implant placement sites in the anterior maxillary region. In the study group, 10 implants were inserted using socket shield technique, while in control group, 10 implants were inserted using conventional immediate placement technique. All patients received immediate and 6 months post-operative CBCT to assess horizontal bone loss, vertical bone loss, and measurement of bone density. Implant stability quotients (ISQs) was measured immediately, 1st, 3rd and 6 months post-operatively.

Detailed Description

Unrestorable tooth extraction with immediate implant placement is considered one of the best treatment options in restoring the esthetics and function. Extraction socket resorption is considered a challenging procedure when it involves the esthetics zone. The preservation of the entire attachment apparatus for complete preservation of the alveolar ridge makes socket shield technique a promising procedure that helps to maintain anatomy, esthetics and function. Socket shield technique, eliminate the negative consequences of bone resorption of the buccal plate of bone; leading to maintaining hard and soft tissue contours and provides a perfect pleasing esthetic result with good function. It is a highly promising technique in terms of maintaining pink and white esthetics through preservation of the interdental papilla during preparation of the interdental socket shield. It is considered a minimally invasive surgical procedure and offers the advantages of immediate implant placement.

Registry
clinicaltrials.gov
Start Date
September 16, 2019
End Date
September 7, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Endodontic or non-endodontic treated un-restorable remaining root/ tooth related to maxillary anterior teeth.
  • Healthy adult patients \> 20 years old (ASAI, II) .
  • Adequate oral hygiene.
  • Intact periodontal tissues.

Exclusion Criteria

  • Periapical or periodontal active infection involving the teeth/root to be extracted (as excluded by radiographic examination).
  • Medically compromised patients (ASA III, IV, V).
  • Patients receiving chemotherapy or radiotherapy.
  • Heavy smokers,alcohol or drug abuse.
  • Patients with parafunctional habits such as bruxism, clenching, excessive gum chewing, lip or fingernail biting.

Outcomes

Primary Outcomes

Vertical bone loss

Time Frame: six month post-operative

Using cone-beam computed tomography

Horizontal gap

Time Frame: six month post-operative

Using cone-beam computed tomography

Bone density

Time Frame: six month post-operative

Using cone-beam computed tomography

Implant stability

Time Frame: six month post-operative

Using osstell

peri-implant probing depth

Time Frame: six month post-operative

using periodontal probe

Study Sites (1)

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