A Non-Interventional Study to Document the Use of Straumann BLX Implants in Daily Dental Practice
概览
- 阶段
- 不适用
- 干预措施
- 未指定
- 疾病 / 适应症
- Surgical Operation With Implant of Artificial Internal Device
- 发起方
- Institut Straumann AG
- 入组人数
- 153
- 试验地点
- 1
- 主要终点
- Implant survival rate at one year post implant placement
- 状态
- 已完成
- 最后更新
- 3个月前
概览
简要总结
Prospective, multi-center, non-interventional observation to document the success and survival rates of Straumann BLX Implants used for tooth replacement in cleared indications up to 1 year after implant placement
详细描述
Objective of the study is to confirm the safety and performance of Straumann BLX Implants used for tooth replacement in cleared indications up to 12 months after implant placement. Implants used are Straumann® BLX Implant Roxolid® SLActive®. Regular Base (3.5 mm): implant diameters 3.75 and 4.5mm, in lengths 6, 8, 10, 12,14, 16 and 18 mm Wide Base (4.5 mm): diameter 5.5 mm in lengths 6, 8, 10 and 12 mm
研究者
入排标准
入选标准
- •Patients seeking an implant supported restoration
- •all patients with conditions that are in accordance with the IFU
- •Patients must provide their informed consent for study participation and must be willing and able to attend control visits
- •Patients need to be at least 18 years old
排除标准
- 未提供
结局指标
主要结局
Implant survival rate at one year post implant placement
时间窗: 12 months follow-up period after implantation
Measured in percent
Implant success rate at one year post implant placement
时间窗: 12 months follow-up period after implantation
Measured in percent
次要结局
- Prosthetic success at 12 months post implant placement(12 months follow-up period after implantation)
- Prosthetic survival at 12 months post implant placement(12 months follow-up period after implantation)