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临床试验/NCT06657651
NCT06657651Enrolling By Invitation不适用

Autogenous Dentine Derived Barrier Membrane Versus Extended Platelet Rich Fibrin Membrane in Immediate Implant Placement

Mansoura University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年6月30日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
40
试验地点
1
主要终点
Implant stability

研究概览

简要总结

forty patients will be selected from the outpatient's clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University for replacement of non-restorable tooth in posterior mandibular area.

Patients' Grouping:

The patients will be randomly divided into two equal uniform groups each consists of 20 patients:

Group A:

20 patients with non-restorable mandibular molar tooth will be treated with an immediately placed dental implant in conjunction with a dentin-derived membrane from the extracted tooth.

Group B:

20 patients with non-restorable mandibular molar tooth will be treated with an immediately placed dental implant in conjunction with extended platelet rich fibrin membrane.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Age above 18 years
  • Non-restorable mandibular molar tooth that needs dental extraction & guided bone regeneration for immediate implant placement.
  • Acceptable inter-arch space for the future prosthesis.
  • Patient medically free from systemic diseases that absolutely contraindicate implant surgery.
  • Cooperative patient with high motivation and acceptable oral hygiene.
  • Free from history of bruxism / parafunctional habits.

排除标准

  • Local and / or systemic conditions that interfere with the procedure.
  • Pregnancy.
  • Uncooperative patients.
  • Patient had undergone in the past 12 months radiation therapy to the head and neck area.

结局指标

主要结局

Implant stability

时间窗: 1 year

Osstell will be used to record implant stability at the placement time, 3, 6 and 12 months after surgery.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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