Computer - Guided Inferior Alveolar Nerve Lateralization With Simultaneous Prosthetic Driven Implant Placement Will be Performed on 10 Surgical Sides (Mandibular Quadrants) to Evaluate the Postoperative Neurosensory Disturbances Following Guided Inferior Alveolar Nerve Lateralization
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: Guided Inferior Alveolar Nerve Lateralization with Simultaneous Implant Placement.
- Who it may be relevant to
- Registry conditions: Neurosensory Function of Inferior Alveolar Nerve. Basic parameters: 30 years — 75 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 →
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Official title
Computer - Guided Inferior Alveolar Nerve Lateralization With Simultaneous Prosthetic Driven Implant Placement
Overview
The aim of this clinical trial is to primarily evaluate the postoperative neurosensory disturbances following guided inferior alveolar nerve lateralization with simultaneous implant placement in 10 surgical sides (mandibular quadrants distal to the mental foramen) either in males or females with age range from 30 to 75 years. The main questions it aims to answer are: 1. Will the postoperative neurosensory disturbances after the surgical intervention fade out and if not, will it be annoying to the patient? 2. Can we consider inferior alveolar nerve lateralization efficient substitute to short implants? 3. will the inserted implants going to be properly ossteointegrated at the site of osteotomy for lateralization?
Interventions
- Procedure Guided Inferior Alveolar Nerve Lateralization with Simultaneous Implant Placement
All patients will be operated on under general anesthesia. A para-crestal incision will be done and a mucoperiosteal flap will be reflected exposing the alveolar ridge and the buccal cortex. The surgical guide will be fitted and fixed in place and the outline of the window will be drawn by the aid of the surgical guide using the piezotome then the guide will be removed. Once the osteotomy is completed the bone window will be mobilized for exposure of the neurovascular bundle. The diamond tips wi
Primary outcome measures
- clinical neurosensory testing of the inferior alveolar nerve function [Time frame: Postoperatively 1 week, 1 month, 3 months, 6 months]
Eligibility criteria
Inclusion criteria
- Atrophic mandibular ridges distal to the mental foramen with residual alveolar bone height ≤ 8 mm above the IAN.
- The width of the alveolar ridge ≥ 6 mm, 3mm down from the alveolar crest.
Exclusion criteria
- All patients suffering from any systemic disease that may contraindicate implant surgery or affect bone healing and osseointegration of implant.
- Previous history of bone augmentation or implant placement in the site planned for nerve lateralization.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Faculty of Dentistry, Tanta University, Egypt — Tanta
Identifiers
NCT: NCT06961045 · OS 4-24 2184