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临床试验/NL-OMON35044
NL-OMON35044已完成不适用

Treatment of peri-implant mucositis; A randomized placebo controlled clinical study - Treatment of peri-implant mucositis

niversitair Medisch Centrum Groningen0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30

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
18 至 99(—)

入选标准

  • 1) The patient is >=18 years of age;
  • 2) The patient has at least one endosseous implant in the oral cavity with clinical signs of peri-implant mucositis. Peri-implant mucositis is defined as bleeding of the peri-implant mucosa on probing, with no signs of loss of supporting bone;
  • 3) The implants have been exposed to the oral environment for at least one year;
  • 4) The patient is capable of understanding and giving informed consent.

排除标准

  • 1) Medical and general contraindications for the interventions;
  • 2) A history of local radiotherapy to the head and neck region;
  • 3) Diabetes;
  • 4) Patients who are allergic to chlorhexidine;
  • 5) Systemic use of antibiotics during the last 3 months;
  • 6) Long-term use of anti-inflammatory drugs;
  • 7) Incapability of performing basal oral hygiene measures as a result of physical or mental disorders;
  • 8) Active, uncontrolled periodontal pathology of the remaining dentition.
  • 9) Local use of antibiotics or use of other anti-septic / antimicrobial therapies in the oral cavity during the last 3 months;
  • 10) Use of mouthrinses during the last 6 weeks or during the course of the study;
  • 11) Implants placed in skin grafted areas;
  • 12) Peri-implantitis;
  • 13) Implant mobility;
  • 14) Implants at which no surface can be identified where proper probing measurements can be performed;
  • 15) Previous treatment of peri-implant mucositis lesions during the last 6 months.

研究者

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