NL-OMON42142已完成不适用
The regenerative surgical treatment of intra-bony peri-implantitis defects with Endobon® (test) versus an established bovine derived bone mineral (control) - Endobon versus BioOss
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64（—）
入选标准
- •During surgical exploration an intra-bony component of at least 3 mm at the deepest point must be present.
- •The defect should have a minimum of 3 osseous walls (a circumference of the osseous defect of at least 270 degrees). Only 3 and 4 wall intraosseous defects will be included.
- •The defect must not be wider than 4 mm and the defect angle must be less than 35 degrees from axis of implant.
排除标准
- •Subjects with diabetes mellitus (HbAlc >= 6.5%)
- •Subjects taking corticosteroids or other anti-inflammatory prescription drug
- •Subjects taking medications known to induce gingival hyperplasia
- •Subjects must not be allergic to penicillin or metronidazole
- •Subjects with a history of taking systemic antibiotics in the preceding month
- •Subjects must not be pregnant or lactating
- •Implants placed in grafted bone or previously augmented with bone substitute or other type of regenerative material
- •If stability of the Endobon® granules or control granules cannot be accomplished in the defect
- •Failure of obtaining soft tissue closure
- •Mobile implants
研究者
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