JPRN-UMIN000013353已完成未知
Randomized, controlled, clinical trial to demonstrate non-inferiority of early loading compared to conventional loading of modSLA Implants placed in single tooth gaps - Clinical trial study of modSLA Implant
Straumann Japan K.K.0 个研究点目标入组 74 人开始时间: 2014年3月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 74
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional,observational
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
- •Systemic exclusion criteria 1. Patients with the systemic disease that would interfere with dental implant therapy (Blood poisoning, weakened immune system, diabetes mellitus, etc--) 2. Patients with the following disease which are applicable to any contraindi-cations or principle contraindications for oral surgery procedures 2-1. Patients who are suffering from a serious internal medical problem such as cardiac infraction or cerebral infraction, uncontrollable endo-crine disorders 2-2. Patients who are suffering from a metabolic bone disease, tem-poromandibular joint disorders, maxillary and mandibular growth not completed, treatable changes in the oral mucosa, local root remnants, xerostomia, patients on bisphosphonate medication 2-3. Patients who are suffering from an inadequate wound healing ca-pacity, prolonged therapy-resistant functional disorders, illnesses re-quiring periodic use of steroids, and who has an irradiation history 2-4. Patients who are having an uncontrolled bleeding disorders, antico-agulation drugs/hemorrhagic diatheses 2-5. Patients who are suffering from psychoses, drug or alcohol abuse, titanium allergy 3. Patients who smoke >10 cigarettes per day 4. Subjects who have participated in another clinical trial within 30 days be-fore obtaining the consent for participating in this trial, or who expect to participate in any other investigational drug or device study during the conduct of this trial 5.Patients who can not follow the instruction from principal investigator or investigator 6.Conditions or circumstances, in the opinion of the Investigator, which would prevent completion of study participation or interfere with analysis of study results 7.Pregnant or breastfeeding women, and women who desire to get preg-nant during clinical study or who has a possibility of it 8.Patients who are uncooperative
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