JPRN-jRCTs072210054暂停2 期
Safety and efficacy of allogeneic bone as a bone filling material for sinus floor augmentation
Ohba Seigo0 个研究点目标入组 10 人开始时间: 2021年8月27日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 暂停
- 发起方
- 入组人数
- 10
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
- >= 20age old 至 < 90age old(—)
- 性别
- All
入选标准
- •1. Patients who have a preference to receive a dental implant treatment for missing tooth in the maxillary posterior region.
- •2. Patients whose alveolar bone volume are insufficient for ideal implant placement, and are required the sinus floor augmentation for the dental implant placement.
- •3. Patients who can personally provide written consent at their own free will after being receiving a thorough explanation of the study and fully understanding their participation in the study.
排除标准
- •1. Patients with problem in judgement.
- •2. Patients with drug hypersensitivity such as allergy.
- •3. Women who are or may be pregnant or lactating women.
- •4. Patients who are participating in another clinical study.
- •5. Patients are immunocompromised with severe diabetes or severe liver or renal dysfunction.
- •6. Patients with severe peptic ulcer or cardiovascular or respiratory diseases and disorders,
- •7. Smokers
- •8. Patients receiving therapies with anti-resorption drugs such as bisphosphonate which affect bone metabolism .
- •9. Partients who are judged to be inappropriate to participate the study by the principal or cooperative doctors.
研究者
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