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临床试验/JPRN-UMIN000020398
JPRN-UMIN000020398已完成2 期

Regenerative medicine using bone marrow-derived mesenchymal cells for maxillomandibular bone defect. - Tissue-Engineered Osteogenic Material for maxillomandibular bone defect (TEOM).

agoya University Hospital0 个研究点目标入组 4 人开始时间: 2016年1月15日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
4

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Patients with bone defect as a result of periodontitis 2. Patients for whom surgical procedure is prohibited e.g, severe heart disease, congenital coagulation factor deficiency, leukemia, dialysis, end-stage malignant tumor 3. Patients with or with a history of infection 4. Patients with diabetes that is not well-controlled 5. Patients taking bisphosphonates for more than 3 months or denosumab for more than 6 months before the consent 6. Patients with or with a history of malignant tumor 7. Patients taking steroids or immunosuppressive drugs who cannot stop such medication for 4 weeks after trial intervention 8. Patients in a serious condition of certain diseases 9. Patients with difficulty in bone marrow aspiration 10. Patients from whom a sufficient amount of blood cannot be taken for PRP preparation 11. Patients with contraindications to local anesthetics 12. Patients with a history of hypersensitivity to antibiotics, antifungals, thrombin products, or bovine blood-derived products 13. Patients taking hemocoagulase products, tranexamic acid products, or aprotinin products 14. Female patients who are pregnant, suspected to be pregnant, breastfeeding, or those who do not agree to practice contraception 15. Any other patients whom the trial investigator deemed ineligible to this study

研究者

发起方
agoya University Hospital

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