NCT07827950已完成不适用
Clinical Assessment of the Efficacy of Amy Check Versus Osstell Regarding the Accuracy of Implant Stability Measurements When Inserted With Graftless Closed Sinus Lifting: A Randomized Controlled Clinical Trial
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- implant stability
研究概览
简要总结
The aim of the study is to compare clinically the efficacy of Amy check device versus Osstell device in evaluating the implant stability of implants placed simultaneously with transcrestal sinus lifting.
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
- 否
入选标准
- •Patient age should be > 18 years of age.
- •Patients included are ASA I and ASA II.
- •Both males and females will be included in the study.
- •Patients with need of tooth replacements in the maxillary premolar and molar area where the residual alveolar bone height ranges from 4-7 mm. 5)Compliance with all requirements in the study and signing the informed consent.
排除标准
- •Patients with immunological diseases or diseases affecting bone healing.
- •Patients suffering from uncontrolled systemic diseases.
- •Patients with active acute infection related to the planned implant site, maxillary sinusitis or pathosis.
- •Patients with parafunctional occlusal habits.
- •Patients with bad oral hygiene.
- •Patients who are alcohol and drug abusers.
- •Patients who smoke.
研究组 & 干预措施
control group
Active Comparator
干预措施: Implant with sinus lifting (Other)
Group A (Study Group)
Active Comparator
干预措施: Implant with sinus lifting (Other)
结局指标
主要结局
implant stability
时间窗: 12 months
次要结局
未报告次要终点
研究者
Dina yousry
Assistant professor
Misr International University
研究点 (1)
Loading locations...
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