PACTR201610001197438Other未知
Evaluation of the stability of short implants in the posterior maxilla and the posterior mandible using the Periotest: controlled clinical trial
Faculty of Oral and Dental Medicine, Cairo University0 个研究点目标入组 30 人开始时间: 2015年7月11日最近更新:
试验速览
- 阶段
- 未知
- 状态
- Other
- 发起方
- 入组人数
- 30
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 Year(s) 至 40 Year(s)（—）
- 性别
- All
入选标准
- •1. Any partially edentulous patient missing teeth in the posterior area requiring 1
- •to 2 dental implants.
- •2. Patient age: 18 years or older
- •3. Able to sign an informed consent form.
- •4. Patients with no systemic diseases.
- •5. Patients who are cooperative, motivated, and hygiene conscious.
- •6. The recipient site of the implant should be free from any pathological
- •conditions.
- •7. Vertical bone heights at implant sites have to be 8.5 - 10 mm above the mandibular
- •canals and 7.5 - 9 mm below the maxillary sinuses.
- •8. Bone thickness has to be at least 6 mm.
排除标准
- •1. Systemic contraindications to implant surgery
- •2. Patients in the growth stage with partially erupted teeth
- •3. Patient subjected to irradiation in the head and neck area
- •4. Immunosuppressed or immunocompromised
- •5. Patient treated or under treatment with intravenous amino-bisphosphonates
- •6. Patients with untreated periodontitis
- •7. Patients with poor oral hygiene and motivation
- •8. Uncontrolled diabetes and heavy smokers
- •9. Pregnant or nursing
- •10.Substance abuse
- •11. Psychiatric problems or unrealistic expectations
- •12. Lack of opposite occluding dentition in the area intended for implant
- •13.Acute or chronic infection/inflammation in the area intended for implant
研究者
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