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临床试验/NCT04489654
NCT04489654Unknown不适用

Evaluation of Immediate Implant Placement With a Modified Socket Shield Technique Using Xenogenic Bone Graft. (a Randomized Controlled Clinical Trial) CLINICAL TRIAL)

Alexandria University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2019年7月20日最近更新:
适应症

试验速览

阶段
不适用
入组人数
16
试验地点
1
主要终点
primary and secondary implant stability measurement

研究概览

简要总结

Adequate bone volume and a proper aesthetic outcome have become the main focus of interest in implant dentistry. Alveolar bone resorption is a natural course occurring after tooth removal. Partial extraction therapy through root preservation has been reported to help in bone maintenance at the extraction site. In 2010, Hurzeler et al. evaluated a new approach, at that time, called socket shield technique. Han et al. in 2018 reported the modification of this technique and leaving the jump gap between the shield and the implant non-grafted. The importance of bone grafting of the gap between the implant and the labial shield in improving quality of regenerating bone and prevention of the soft tissue ingrowth has been described. Thus the hypothesis, of improving the modified socket shield technique by bone grafting could be tested.

Aim of this study is to evaluate the clinical and radiographic outcomes of using xenogenic bone graft on outcome of immediate dental implant placement using the modified socket shield technique.

详细描述

16 patients who are admitted to the outpatient clinic of Oral and Maxillofacial Surgery Department, are divided into two study groups. Control group will receive an immediate implant with modified socket shield technique. Test group will receive immediate implant with modified socket shield and deproteinized bovine bone mineral (DBBM) put in the buccal gap. Outcome measurement is primary and secondary implant stability measurement and CBCT evaluation.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age more than 18 years old irrespective of the gender
  • One or more of non-restorable (fractured or decayed) tooth/teeth in the upper aesthetic regions (incisors, premolars).
  • Free from periodontal diseases.
  • Sufficient bone volume to allow placement of an implant.
  • Ability to read and sign an informed consent form
  • Adequate buccolingual width to allow for a buccal gap presence.

排除标准

  • A medical history that contraindicates oral surgical treatment (uncontrolled/untreated diabetes mellitus, immuno-compromised status, radio/chemotherapy of the oral and maxillofacial region, treatment with oral and/or intravenous amino-bisphosphonates).
  • Untreated periodontal disease.
  • Vertical root fractures on the buccal aspect.
  • Tooth /teeth with horizontal fractures below bone level.
  • Tooth /teeth with external or internal resorptions.

结局指标

主要结局

primary and secondary implant stability measurement

时间窗: 4 months

Implant stability measured in units ISQ is concluded through a clinical evaluation using ostell

次要结局

  • Bone mineral density(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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