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临床试验/NCT06650280
NCT06650280已完成不适用

Assessment of Osseointegration of Dental Implants with Three Different Coatings for Early Loading Purpose and Marginal Bone Loss in the Posterior Maxilla. a Randomized Clinical Trial

October University for Modern Sciences and Arts1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2023年2月1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
45
试验地点
1
主要终点
rapid osseintegration

研究概览

简要总结

The study will assess early osseointegration of dental implant with three different coating materials through secondary implant stability

详细描述

Dental implants with sandblasted acid itched coating, nano-hydroxyapatite coating, and hyalouronic acid coating will be placed in the posterior maxilla to restore a missing tooth. Implant stability by the use of Ostell will be measured immediately post-operative, 4, 6, and 12 weeks post-operative.

marginal bone loss around the implants will be compared immediately after final restoration delivery and after one year

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
Single (Participant)

入排标准

年龄范围
18 Years 至 49 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients with missing at least one maxillary posterior tooth
  • •Patients free from any systemic disease
  • •Patients who approve to be included in the trial and sign the informed consent
  • •Patients with no intra-bony defect.
  • •Adults aged 18 years old and above

排除标准

  • •Patients who are allergic to titanium
  • •Heavy smoker patient
  • •Patients receiving chemotherapy or radiotherapy
  • •Patients who refused to be included in the trial

研究组 & 干预措施

sandblasted acid etched group

Experimental

sandblasted acid etched coated implants will be allocated to this arm

干预措施: sandblasted acid etched (Other)

nano-hydroxyapatite group

Active Comparator

nano-hydroxyapatite coated implants will be allocated to this arm

干预措施: nano-hydroxyapatite (Other)

hyaluronic acid group

Experimental

hyaluronic acid coated implants will be allocated to this arm

干预措施: Hyaluronic Acid (HA) (Other)

结局指标

主要结局

rapid osseintegration

时间窗: immediately post-operative, 4, 6, and 12 weeks post-operative

rapid osteointegration of dental implants will be evaluated by the use of Ostell device which measures primary and secondary stability expressed as ISQ measures ranging from zero till 90

次要结局

  • marginal bone loss(immediately after final restoration delivery and one year post-operative)

研究者

发起方
October University for Modern Sciences and Arts
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohamed Hamdy Mahmoud Ismail

Lecturer of Oral & Maxillofacial Surgery

October University for Modern Sciences and Arts

研究点 (1)

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