KCT0008983招募中Unknown
Comparison of novel tapered implants with long neck design(ARi® ExCon) and conventional tapered implants(XPEED AnyRidge) in atrophied alveolar ridges: a randomized controlled clinical trial
适应症
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 入组人数
- 40
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
- 20(Year) 至 o Limit（—）
- 性别
- All
入选标准
- •1) Adult males and females, aged 20 years or older, with completed growth of the jaw, who are systemically amenable to surgical treatment of implant placement.
- •2) Subjects who require single-tooth implant placement to restore esthetic and masticatory function due to loss of one or more of the incisors or premolars of the upper or lower jaw.
- •3) Subjects with suitable anatomical structures and dental conditions for implant placement.
- •- On CBCT image evaluation, there are no specific pathologies in the edentulous area and the anatomical structure is suitable for implant placement.
- •4) Subjects of antagonist teeth (either natural teeth or implant prosthesis).
- •5) Subjects who do not have plans for implant placement in adjacent teeth within 6 months following implant restoration.
- •6) Subjects who voluntarily consent to participate in the clinical trial and are willing and able to comply with the study protocol.
排除标准
- •1) General exclusion criteria
- •(1) Women of childbearing potential.
- •(2) Subjects with a history of myocardial infarction within the last 6 months.
- •(3) Subjects with uncontrolled medical conditions (hypertension, diabetes, osteoporosis, thyroid disease).
- •(4) Subjects with bleeding disorders.
- •(5) Subjects with hypersensitivity to implant materials.
- •(6) Subjects with a smoking habit of more than 20 cigarettes per day.
- •(7) Subjects with dependence on alcohol or drugs.
- •(8) Subjects whose participation in the study is deemed inappropriate by the researcher for ethical reasons or because it may affect the results of the study.
- •2) Dental-related exclusion criteria
- •(1) Subjects with severe bruxism, clenching, or other harmful oral habits.
- •(2) Subjects with contraindications for oral surgeries (e.g., inadequate wound healing capacity, poor oral hygiene, severe dry mouth).
- •(3) Less than 8 weeks after tooth extraction.
- •(4) Subjects requiring treatment in the edentulous area or its vicinity (adjacent teeth, antagonist teeth).
- •- Have mucosal disease (e.g., lichen planus).
- •- Presence of acute infection or active periodontitis or gingivitis.
- •- Extensive bone loss due to periodontal disease requiring extraction of adjacent teeth.
- •(5) Subjects with a history of bone grafting or alveolar ridge preservation at the edentulous area within 6 months of the procedure.
- •(6) Subjects with abnormal occlusion in the posterior region.
- •(7) Subjects with pathological conditions like tumors or osteomyelitis, or who have previously undergone removal surgery for such conditions in the edentulous area or elsewhere in the oral cavity.
- •(8) Periodontal pocket depth of adjacent natural teeth exceeds 6 mm.
研究者
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