Temporary push-on Rings of Antimicrobial Alloys for Transmucosal Implant Abutment Systems: a Randomized Clinical Study on Early and Mature Biofilm Formation
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 33
- 试验地点
- 1
- 主要终点
- Change in total bacterial load formed on the removable rings of each material
研究概览
简要总结
This in-vivo study investigates early (48h), mature (2 weeks) and long-term (3 months) biofilm formation and composition on temporary push-on cones (exchangeable conical rings) made of noble-alloy-based materials (Pagalinor, PA) in comparison to Titanium-6Aluminum-7Niobium alloy (TAN) presently used in the transmucosal portion of dental implant abutments.
详细描述
Oral biofilm (dental plaque) consists of bacteria and their metabolic products as well as saliva components and food residues. It is recognizable as a tough and structured coating on teeth and artificial surfaces within the oral cavity. Plaque development is a physiological process that begins immediately after cleaning of the oral surface. If the biofilm is not removed by daily oral hygiene, it continues to mature while changing the structure and its microbial composition.
Implant restorations comprise the osseous implant portion predominantly manufactured from titanium alloys, the transmucosal implant portion (in most implant systems as a separate abutment), and the clinical crown, which is in most systems extraorally cemented on an abutment and screw-retained onto the implant. According to current knowledge, microbial colonization of the implant abutment surface plays a significant role in the aetiology of peri-implantitis.
This study investigates the antibacterial potential of a temporary push-on cone (conical ring) that could reduce the risk of bacterial related peri-implant diseases due to decreased biofilm susceptibility, compared to current available transmucosal materials, in the short- and long-run. The test material Pagalinor®2 (PA) is an established material in dental medicine and has proven to accumulate least biofilm in an in-vivo biofilm sampling model using removable splints. The control material consists of the current transmucosal implant abutment material Titanium-6Aluminum- 7Niobium alloy (TAN). The push-on rings are designed for repeated application along the transmucosal implant abutment portion with high precision fit and will allow biofilm sampling in the natural implant environment. Profound insight into the native homeostasis of biofilm formation will be obtained and therefore enhance the knowledge about long-term tissue response.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- Double (Participant, Investigator)
盲法说明
Double-blinded with the patient not knowing which material is placed, and the investigator and laboratory technicians have no information about the ring material.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Informed Consent signed by the subject
- •Presence of one or more bone level titanium implant prior to insertion of the final restoration
- •No systemic illness
- •No heavy smoking (smoking <10 cigarettes/day)
- •No pregnancy
- •No active periodontitis (probing pocket depth ≤4 mm)
- •No pharmacological treatment or antibiotic therapy during or up to three months before the study
排除标准
- •Systemic illness (e.g. Diabetes)
- •Heavy smoking (smoking >10 cigarettes/day)
- •Known or suspected non-compliance, drug or alcohol abuse
- •Pregnancy
- •Active periodontitis (probing pocket depth >4 mm)
- •Pharmacological treatment or antibiotic therapy during or up to three months before the study
研究组 & 干预措施
Pagalinor®2 (PA) test arm
All patients will wear both the test and control ring material for a within-subject comparison. Ideally, biofilm sampling can be performed in a split mouth design (randomly allocated materials within subjects) with one patient having two implants for placing the test and the control material at the same time. In addition, patients providing one implant, will receive test and control push-on rings in a randomly assigned order, so that both materials are assessed in a consecutive manner.
干预措施: Rings made of PA (test) (Device)
Titanium-6Aluminum- 7Niobium alloy (TAN) control arm
All patients will wear both the test and control ring material for a within-subject comparison. Ideally, biofilm sampling can be performed in a split mouth design (randomly allocated materials within subjects) with one patient having two implants for placing the test and the control material at the same time. In addition, patients providing one implant, will receive test and control push-on rings in a randomly assigned order, so that both materials are assessed in a consecutive manner.
干预措施: Rings made of TAN (control) (Device)
结局指标
主要结局
Change in total bacterial load formed on the removable rings of each material
时间窗: at 48 hours after ring placement, 2 weeks after ring placement and 3 months after ring placement
Quantification of the bacterial load formed on the removable rings of each material by quantitative real-time PCR (qPCR) using primers specific to highly conserved regions of bacterial 16S rRNA genes.
次要结局
- Change in bleeding on probing (BoP)(at baseline, 2 weeks after ring placement and 10 weeks after ring placement)
- Change in noninvasive laser doppler flowmetry(at baseline, 2 weeks after ring placement and 10 weeks after ring placement)
- Change in the cells of the peri-implant soft tissue(at 2 weeks after ring placement)
- Change in bacterial composition (taxonomic diversity) between different materials at various time points by using metagenomic sequencing analysis(at baseline, 2 weeks after ring placement and 10 weeks after ring placement)
- Change in probing pocket depth (PPD) in mm(at baseline, 2 weeks after ring placement and 10 weeks after ring placement)