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临床试验/NCT04017429
NCT04017429撤回不适用

Treatment of Grade III Furcation Defects in Teeth With Low Interproximal Crestal Bone Height, With and Without Osteoplasty, in Conjunction With Open Flap Debridement

University of Oslo1 个研究点 分布在 1 个国家开始时间: 2019年10月15日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Sites with no signs of inflammation

研究概览

简要总结

Teeth with furcation grade III defects will be treated with open flap debridement, with or without osteoplasty. The study is designed to examine the effect of osteoplasty in the treatment of teeth with furcation grade III defects with open flap debridement.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Periodontal disease stage III or IV according to 2018 criteria
  • Undergoing periodontal therapy (active or supportive) and present 1 or more pair of bilateral mandibular molars affected by furcation involvement grade III with PPD>4mm, and the furcation fornix must be above a tangential line from the distal to mesial interproximal crestal bone level on bitewing radiographs
  • Competent to give consent

排除标准

  • Previous radiotherapy to the jaws, current use of chemotherapy, systemic long-term corticosteroid treatment
  • Present or past use of bisphosphonate treatment
  • Pregnant or nursing subjects
  • Patients classified as > class II according to ASA classification
  • Previous surgical therapy of included furcation defects
  • Inhability to comprehend and respond to the quality of life questionnaire
  • Dental restorations or prosthesis involving the furcation area
  • Root fractures or suspected fractures/infractions
  • Caries lesoins in the furcation area
  • No systemic antibiotic treatment within 3 months prior to intervention

结局指标

主要结局

Sites with no signs of inflammation

时间窗: 24 months after treatment

Proportion of sites without inflammation, defined as no BoP or PPD\>4mm following treatment

次要结局

  • Loss of clinical attachment level(24 months after treatment)
  • Number of participants with caries lesions(24 months after treatment)
  • Radiographic changes(24 months after treatment)
  • Changes in patient-reported quality of life (QoL)(Preoperatively compared to 12 months after treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Anders Verket

Associate Professor, PhD

University of Oslo

研究点 (1)

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