KCT0003004已完成未知
A single center, Randomized, Patient-Evaluaor blind, Paired-Comparison Clinical study to evaluate the efficacy and safety of treatment with TDI-SM1 as compared to TXT2530 in correction of periodontium regeneration
Spenser Biomedical Technology0 个研究点目标入组 25 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 25
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 18(Year) 至 o Limit（—）
- 性别
- All
入选标准
- •1. Healthy men and women over 20 years
- •2-3. Patients with bilateral, fully horizontal or mesioangular impacted, mandibular third molars
- •4. Present minimum 3mm-sized bony defect in the distal surface of the mandibular second molar and minimum 5mm-sized periodontal pocket depth in the distal surface of the mandibular second molar at the time of extraction
- •5. Patient's signed impacted consent form
排除标准
- •1. age <20 years
- •2. Patients with partially impacted mandibular third molar
- •3. Smokers
- •4. Patients with any systemic disease
- •5. Patients receiving irradiation on head and neck area
- •6. Patients with malignant cancer history
- •7. Patients with any oral mucosal disease
- •8. Patients with poor oral hygien
- •9. Pregnant and nursing mothers
研究者
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