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Labial Bone Thickness Around Immediate Implants in the Esthetic Zone Following a Novel Socket Evaluation System

Observational Immediate Implant Placement

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Immediate implants with bone grafts, Immediate implant placed without bone grafts or any grafting substitutes in the labial gap.
Who it may be relevant to
Registry conditions: Immediate Implant Placement. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

a Novel Socket Evaluation System and Its Impact on Bone Formed Labial to Bone Immediate Anterior Implants. A 1-year Clinical Trial.

Overview

The anterior maxilla is a particularly challenging area for immediate implant placement due to its thin buccal bone walls. These walls are more susceptible to resorption after tooth extraction, which can lead to significant bone loss and inadequate support for an implant. However, Different socket dimension may affect the amount of bone formed labial to the implant, regardless of the garfting procedure.

Detailed description

Bone formation labial to the immediate implant is not related to the initial thick- ness of the labial plate of bone, rather than the initial labio-palatal socket dimension. this study aims to evaluate the bone formed labial to the implant following a Novel Socket Evaluation System.

Interventions

  • Procedure Immediate implants with bone grafts
    Immediate implants with bone grafts
  • Procedure Immediate implant placed without bone grafts or any grafting substitutes in the labial gap
    Immediate implant placed without bone grafts or any grafting substitutes in the labial gap

Primary outcome measures

  • Bone labial to the implant [Time frame: one year]
Secondary outcome measures (1)
  • Bone area at the Interproximal component [Time frame: preoperative]

Eligibility criteria

Inclusion criteria

  • Immedaite implants in anterior maxilla
  • thick gingival phenotype
  • intact but thin labial plate of bone (≤1mm)
  • sufficient apical bone to attain implant primary stability (a minimum of 35 Ncm insertion torque)

Exclusion criteria

  • smokers
  • pregnant women
  • patients with systemic disease
  • patients with parafunctional habits such as bruxism or clenching,
  • infected socket
  • periapical pathosis
  • history of radiotherapy or chemotherapy within the past 2 years.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • International Dental Clinic Educational centre — Cairo

Identifiers

NCT: NCT06648135 · IDCE 14

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗