Immediate Dental Implants in The Upper Anterior Region

April 21, 2024 updated by: Mansoura University

Maxillary Anterior Teeth Replacement With Immediate Dental Implants Utilizing Vestibular Socket Therapy Versus Ice Cream Cone Technique

The aim of the study will be to evaluate maxillary anterior teeth replacement with immediate dental implant utilizing vestibular socket therapy versus ice cream cone technique both clinically and radiographically.

Study Overview

Detailed Description

Tooth loss is the endpoint of oral diseases, such as dental caries and periodontitis, and reflects the utilization of dental services during a lifetime .

The incidence of tooth loss has significantly declined at the global levels. However, tooth loss and oral diseases are still a major public health concern worldwide.

In the anterior region, the common reason for tooth loss is due to traumatic injury or congenital anomaly, loss of a single tooth may cause functional and esthetic deficits to the patient. Tooth extraction usually accompanies alveolar ridge resorption along with loss of preexisting tissue morphology.

There is a new developed a post-extraction fresh socket classification system as follows: Type 1: The facial soft tissue and buccal plate of bone are at normal levels in relation to the cement enamel junction of the pre-extracted tooth and remain intact post extraction.

Type 2: Facial soft tissue is present, but the buccal plate is partially missing following extraction of the tooth. Type 3: The facial soft tissue and the buccal plate of the bone are both markedly reduced after tooth extraction. This classification enabled ordering and classifying of post-extraction sockets.

A recently published sub-classification of type 2, now allows even greater clarity to plan regeneration: Type 2 A: Absence of the coronal one-third of labial bone plate of the extraction socket 5mm to 6mm from the free gingival margin. Type 2 B: Absence of the middle to coronal two thirds of the labial bone plate of the extraction socket approximately 7mm to 9mm from the free gingival margin.

Type 2 C: Absence of the apical one-third of the labial bone plate of the extraction socket 10 mm or more from the free gingival margin. For the management of socket defects after extraction numerous techniques have been developed to allow for optimum esthetic and functional outcomes. Among those techniques are ice cream cone technique described by Deniss Tarnow and the more recently introduce vestibular socket therapy (VST) introduced by Abd Salam Elaskary . Deniss Tarnow invented his technique (ice cream cone) to augment the socket with buccal dehiscence, in this technique, socket preservation was done using a collagen membrane shaped into an ice cream cone and placing it inside the extraction socket to cover the dehiscence site and the socket occlusally at the same time.

The regeneration of the buccal plate using the "ice cream cone" technique was possible in the dental extraction and by the immediate implant in an infected site in a case report of a 53 years old patient, and also in a clinical case series. But this technique is only recommended for simple dehiscence and not a wall defect. This technique is not applicable for a completely defective or missing bone wall unless a flap is raised, and (GBR) procedure is performed. Difficulty in placing the membrane as it become softened when exposed to fluid. In 2020 , Abd salam Elaskary , introduced vestibular socket therapy (VST), a novel minimally invasive surgical technique that allowed placement of immediate implant in maxillary class I and class II fresh extraction sockets with or without infective signs.

A 1-cm long vestibular access incision was made using a 15 blade 5-6 mm apical to the mucogingival junction of the socket, exposing the alveolar bone. The vestibular tissues were dissected in a coronal direction to detach the periosteum, forming a sub-periosteal tunnel connecting the vestibular incision to the socket orifice,bone graft was then introduced through the vestibular access incision to augment the labial plate of bone and fill any jumping gap. A flexible cortical membrane of 0.6 mm thickness was inserted and positioned 1 mm apical to the soft tissue margin and secured using two tacks apically. A customized healing abutment was fabricated to cover the implant and seal the socket .

This technique has many advantages : firstly, the nature of the vestibular extraction approach does not cause any trauma, pressure, or laceration to the soft tissue margin, which in turn has a positive impact on enhancing the mid-facial soft tissue levels, as the root was only pushed in an incisal direction through the created 6vestibular pouch, thus minimizing the osteoclastic activity around the socket rim .

, so it overcomes the remodeling sequelae of tooth extraction and to minimize the mid facial peri-implant gingival recession.

Secondly ,the use of a slowly resorbing flexible labial shield allowed for remodeling of the underlying labial bone plate while maintaining the socket dimensions and contours throughout the follow-up period. Thirdly, the membrane fixation, which is known to be pivotal for the GBR stability and regenerative outcomes. and finally connective tissue grafting can be done in type II sockets exhibiting a thin biotype. In these cases, the soft tissue graft counteracted the detrimental effect of the thin gingival phenotype on horizontal bone loss and midfacial mucosal recession.

VST can manage both type I and II socket defects, and could shorten the treatment time by up to two-thirds of that required for bone grafting and delayed implant placement.

Study Type

Interventional

Enrollment (Estimated)

16

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Mansoura, Egypt, 7650001
        • Faculty of Dentistry Mansoura University
        • Contact:
        • Principal Investigator:
          • Mohamed Fa Shoeib, demonstrator

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

inclusion criteria :

  1. Age more than 18 - 40 years.
  2. Patients with missing single tooth or teeth in the esthetic zone.
  3. Patients with buccal wall defect Type 2 A, B sockets (thin labial plate of bone less than 0.5 mm, presence of dehiscence or fenestration).
  4. Good oral hygiene.
  5. Patients willing to be present during the study follow-up intervals.
  6. Patients free from any systemic diseases that may contraindicate implant placement .
  7. Crown height space of at least 8 mm.
  8. Patients without any para-functional habits (bruxism and clenching).

Exclusion Criteria:

  1. Smoking people.
  2. Alcohol or drug abuse.
  3. Pregnancy.
  4. Patients with poor oral hygiene or progressive periodontal disease .

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group A :immediate dental Implants cases with ice-cream cone technique in type 2 socket
immediately placed implants in which the socket defect will be treated utilizing ice cream cone technique by Dennis Tarnow using collagen membrane , allograft bone graft and custom healing abutments
collagen membrane and allograft bone for labial plate augmentation simultaneously with immediate implants placements in maxillary anterior region in the defected type 2 socket , custom healing abutment for soft tissue preservation in ice cream cone group
Experimental: Group B : immediate dental Implants cases with the vestibular socket therapy in type 2 socket
8 immediately placed implants in which the socket defect will be treated utilizing vestibular socket therapy technique using cortical lamina , allograft , bone tacks for fixation and custom healing abutment
cortical lamina fixed by bone tacks and allograft bone for labial plate augmentation simultaneously with immediate implants placements in maxillary anterior region in the defected type 2 socket , custom healing abutment for soft tissue preservation in ice cream cone group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Bone changes
Time Frame: 12 months
bone changes in volume by cone-beam computed tomography (CBCT )radiographically .
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
soft tissue changes
Time Frame: 12 months
evaluation of Probing depth around implants by a graduated dental probe , differences in volume changes by Standard Triangle Language( STL) files superimposition of the arches digitally by etc: Medit software.
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

April 21, 2024

Primary Completion (Estimated)

March 1, 2025

Study Completion (Estimated)

April 1, 2025

Study Registration Dates

First Submitted

April 10, 2024

First Submitted That Met QC Criteria

April 21, 2024

First Posted (Actual)

April 24, 2024

Study Record Updates

Last Update Posted (Actual)

April 24, 2024

Last Update Submitted That Met QC Criteria

April 21, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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