ISRCTN14347002
已完成
未知
The regenerative surgical treatment of intra-bony peri-implantitis defects with Endobon® (test) versus an established bovine derived bone mineral (control) – a pilot study
Academic Center for Dentistry Amsterdam0 个研究点目标入组 25 人2020年2月20日
概览
- 阶段
- 未知
- 干预措施
- 未指定
- 疾病 / 适应症
- 未指定
- 发起方
- Academic Center for Dentistry Amsterdam
- 入组人数
- 25
- 状态
- 已完成
- 最后更新
- 5年前
概览
简要总结
2020 results in https://doi.org/10.1111/clr.13651 (added 11/09/2020)
研究者
入排标准
入选标准
- •1\. During surgical exploration an intra\-bony component of at least 3 mm at the deepest point must be present.
- •2\. 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
- •3\. The defect must not be wider than 4 mm and the defect angle must be less than 35 degrees from axis of implant
- •Note: If the same patient has more than one defect meeting the inclusion criteria only one such defect will be included in the study and the other defects will be treated with standard open flap debridement
排除标准
- •1\. Diabetes mellitus (HbAlc \= 6\.5%)
- •2\. Taking corticosteroids or other anti\-inflammatory prescription drug
- •3\. Taking medications known to induce gingival hyperplasia
- •4\. Allergic to penicillin or metronidazole
- •5\. History of taking systemic antibiotics in the preceding month
- •6\. Pregnant or lactating
- •7\. Stability of the Endobon® granules or control granules cannot be accomplished in the defect
- •8\. Failure of obtaining soft tissue closure
- •9\. Mobile implants
结局指标
主要结局
未指定
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