跳至主要内容
临床试验/NCT04957654
NCT04957654Unknown不适用

A Comparative Study Evaluating Vestibular Socket Therapy in Immediate Implants Using Different Grafting Materials

Mohamed Mofreh Hamada Hamed1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2021年3月16日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
24
试验地点
1
主要终点
changes in facial plate height

研究概览

简要总结

The current research aims at evaluating the outcomes of the vestibular socket therapy in immediate implants using collagen plug, demineralized freeze-dried bone allograft, and deproteinized bovine bone minerals at both radiographic and clinical levels

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 (Outcomes Assessor)

盲法说明

statistician will be blind

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients will be included if they have one or more hopeless teeth without signs of acute infection in the maxillary anterior region.
  • Remaining roots or non-restorable teeth with sufficient bone apically and palatably to allow proper implant positioning with sufficient primary stability.
  • Optimal compliance as evidenced by no missed treatment appointments and a positive attitude towards oral hygiene.
  • Medically free

排除标准

  • Medically compromised patients and systemic conditions precluding implant and periodontal surgery.
  • Smokers, diabetics, pregnant or lactating women.
  • History of chemotherapy, radiotherapy in head and/or neck region.
  • Bisphosphonate therapy

结局指标

主要结局

changes in facial plate height

时间窗: at baseline, 6 and 12 months

Each group will be subjected to: Cone beam computed tomography (CBCT) at baseline, 6 months, and 12months to assess height of labial (facial) plate of bone and implant survival

changes in facial plate thickness

时间窗: at baseline, 6 and 12 months

Each group will be subjected to: Cone beam computed tomography (CBCT) at baseline, 6 months, and 12months to assess the thickness of the labial (facial) plate of bone and implant survival

次要结局

  • changes in peri-implant mucosal level(at baseline, 3rd and 6th months)

研究者

发起方
Mohamed Mofreh Hamada Hamed
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Mohamed Mofreh Hamada Hamed

clinical researcher

Tanta University

研究点 (1)

Loading locations...

相似试验