JPRN-jRCTs072180076已完成1 期
Efficacy of freeze-dried platelet-rich plasma (FD-PRP) in bone engineering: Pilot study - Efficacy of freeze-dried platelet-rich plasma (FD-PRP) in bone engineering
Asahina Izumi0 个研究点目标入组 5 人开始时间: 2019年3月26日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 5
研究概览
简要总结
The purpose of this study is to evaluate the safety and preliminary efficacy of autologous freeze-drying platelet-rich plasma (FD-PRP) on maxillary sinus floor bone augmentation as a preliminary pilot study. 5 patients that required sinus floor augmentation to facilitate the placement of dental implants participated in this study. The primary outcome was a safety verification of triple-concentrated FD-PRP (x3 FD-PRP) and there were no adverse events related to the transplantation of FD-PRP.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 <= 75age old(—)
- 性别
- All
入选标准
- •1. Patients who are partially or fully edentulous, and are required to treat by dental implants for prosthetic rehabilitation.
- •2. Patients who have insufficient bone height and/or width to place the dental implant
- •3. Patients who received the oral health care and maintain the good condition of Plaque Control.
- •4. The age of the patients: 20- to 75-years old
排除标准
- •1. All patients are required to be nonsmokers.
- •2. Patients who have systemic disease, malignances, chronic infections, immune system abnormalities, septicemia, syphilis, HBV, HCV, HTLV-1, HIV, pregnancy, dementia.
- •3. Patients who have disorder of blood coagulation.
- •4. Patients who have hepatitis function disorders, metabolic bone disease or skeletal dysplasia.
- •5. Patients who needs the legal representative.
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