跳至主要内容
临床试验/NCT04590339
NCT04590339已完成不适用

Lateralization of the Inferior Alveolar Nerve After Repositioning of the Bone Window Versus Sticky Bone Augmentation: A Randomized Controlled Clinical Trial

Alexandria University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年10月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
1
主要终点
Clinical assessment of the change in neurosensory function recovery using Brush stroke discrimination test.

研究概览

简要总结

Rehabilitation of edentulous posterior mandibular regions with severe ridge atrophy using implants is subject to anatomical, surgical, and biological difficulties. In many cases, the bone is severely atrophied that sufficiently long fixtures cannot be placed without encroaching on the inferior alveolar nerve (IAN). IANL is defined as the lateralization of inferior alveolar neurovascular bundle posterior to the mental foramen, with preservation of the incisive nerve; exposure and traction are used to deflect the IAN laterally while the implants are placed.

详细描述

This prospective randomized clinical trial will enroll 20 patients with posterior mandibular ridge atrophy. Ten of which will undergo computer guided nerve lateralization with subsequent implant placement and repositioning of the osteomotized bone window and ten patients will undergo computer guided nerve lateralization with subsequent implant placement and sticky bone grafting.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
25 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients suffering from unilateral posterior mandibular edentulism and having < 8 mm of bone above the mandibular canal.
  • •The width of the ridge should be > 4mm.
  • •The patient should be psychologically accepting the implant and the involved procedures.
  • •The patients should have adequate oral hygiene and adequate bone quality.

排除标准

  • •Any absolute contraindication for implant surgery such as uncontrolled diabetes mellitus, blood and/or bleeding disorders, serious osseous defects...etc.
  • •Any relevant systemic disease directly affecting bone metabolism and healing.
  • •Any habits that might reduce the blood flow and retard healing such as heavy smoking and alcoholism.
  • •A history of any grafting procedure at the designated area.
  • •Patient with thick cortical bone buccally and a thin neurovascular bundle.

研究组 & 干预措施

Repositioning the bone window

Active Comparator

Computer guided inferior alveolar nerve lateralization and implant placement with subsequent repositioning of the osteotomized bone window.

干预措施: Guided inferior Alveolar Nerve lateralization (Procedure)

Augmentation using sticky bone

Active Comparator

Computer guided inferior alveolar nerve lateralization and implant placement with grafting around the implant using sticky bone

干预措施: Guided inferior Alveolar Nerve lateralization (Procedure)

结局指标

主要结局

Clinical assessment of the change in neurosensory function recovery using Brush stroke discrimination test.

时间窗: 1 week, 1 month, 3 months and 6 months

Done at 1 week, 1 month, 3 months and 6 months postoperative.

Clinical assessment of the change in neurosensory function recovery using two point discrimination test

时间窗: 1 week, 1 month, 3 months and 6 months

Done at 1 week, 1 month, 3 months and 6 months postoperative.

Clinical assessment of the change in neurosensory function recovery using pin-prick sensation test.

时间窗: 1 week, 1 month, 3 months and 6 months

Done at 1 week, 1 month, 3 months and 6 months postoperative.

Change in neurosensory recovery and sensation regaining over 6 months compared to normal (taken at base line)

时间窗: 1 month, 3 months and 6 months

Electrophysiological test using Mental nerve Blink reflex is done for each patient before surgery(base line), after surgery at 1 month, 3 months and 6 months.

Clinical assessment of the change in neurosensory function recovery using Static light touch detection test.

时间窗: 1 week, 1 month, 3 months and 6 months

Done at 1 week, 1 month, 3 months and 6 months postoperative.

次要结局

  • Implant Success rate(3 months and 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验