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临床试验/NCT06667778
NCT06667778已完成不适用

Effectiveness of Osseodensification in Enhancing Implant Stability and Ridge Expansion in Esthetic Region (a Randomized Controlled Clinical Trial)

Hams Hamed Abdelrahman1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2021年1月12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
发起方
入组人数
18
试验地点
1
主要终点
Change in implant stability

研究概览

简要总结

Dental implants supported restorations have been widely accepted as one of the treatment modalities to replace missing teeth and to restore human masticatory function. Successful osseointegration from the clinical standpoint is a measured by implant stability, which occurs after implant integration. Osseodensification is a bio-mechanical site preparation technique. It utilizes a multi-fluted densifying bur technology that creates and expands a pilot hole without excavating significant amounts of bone tissue through a unique, highly controllable, fast, and efficient procedure with minimal heat elevation.

Aim of the study: Is to evaluate and compare the efficacy of using osseodensification compared to conventional bone expansion in implant stability and ridge expansion.

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
20 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Missing maxillary anterior tooth, having moderate horizontal ridge defect in which the alveolar ridge width is( 3-4) mm, and its height is not less than 10 mm.
  • •Presence of adequate keratinized mucosa.
  • •Patients with good oral hygiene.
  • •Patients are free from any systemic diseases that might affect healing.
  • •Presence of adequate inter-occlusal and mesiodistal space that permits placement of fixed prosthesis.

排除标准

  • •Heavy smokers and bad oral hygiene patients.
  • •Medically compromised patients that affecting placement of implant.
  • •Alcohol or drug abuse.
  • •Pregnant women.
  • •Patients suffering from osteoporosis.
  • •Current chemotherapy or radiotherapy.

研究组 & 干预措施

Study group

Experimental

干预措施: Osseodesification densah burs (Device)

Control group

Active Comparator

干预措施: Microdent (Device)

结局指标

主要结局

Change in implant stability

时间窗: Baseline and 16 weeks

Implant stability will be measured using the Ostell device.

次要结局

  • Change in bone density(Baseline and 16 weeks)
  • Change in ridge expansion(Baseline and 16 weeks)
  • Change in bone loss(Baseline and 16 weeks)

研究者

发起方
Hams Hamed Abdelrahman
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hams Hamed Abdelrahman

Assistant Lecturer of Dental Public Health and biostatistical consultanat

Alexandria University

研究点 (1)

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