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临床试验/NCT06609720
NCT06609720已完成不适用

Evaluation of Autogenous Dentin Graft Versus Demineralized Freeze-Dried Bone Allograft in the Treatment of Class ΙΙ and ΙΙΙ Mandibular Furcation Defects

Tanta University1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2021年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
1
主要终点
Probing pocket depth

研究概览

简要总结

Randomized clinical and radiographic trial

详细描述

Evaluation of Autogenous Dentin Graft versus Demineralized Freeze-Dried Bone Allograft in the Treatment of Class ΙΙ and ΙΙΙ Mandibular Furcation Defects

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
Single (Outcomes Assessor)

入排标准

年龄范围
35 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Presence of class II and/or ΙΙΙ furcation defects in mandibular first or second molars according to criteria outlined by Hamp et. al.
  • Horizontal probing depth ≥3 mm using Naber's probe.
  • Clinical attachment level ≥3 mm measured from cemento-enamel junction (CEJ) till the deepest probing depth.
  • Evidence of radiolucency in the furcation area on panoramic radiograph.
  • Patients who will be assigned for groups (I and II) should present with teeth required for extraction due to advanced periodontal bone loss or other indications such as hopeless wisdom teeth or orthodontic indications or unrestorable fractured teeth as a source for autogenous dentin graft (ADG).

排除标准

  • Medically compromised patients and systemic conditions precluding periodontal surgery.
  • Mandibular first or second molars with root caries or endodontic treatment.
  • Smokers, diabetics, pregnant or lactating women.
  • History of chemotherapy, radiotherapy in head and/or neck region.
  • Bisphosphonate therapy.

结局指标

主要结局

Probing pocket depth

时间窗: Measured at baseline, 6 months and 12 months

According to Ramfjord, clinical parameter measured by UNC periodontal probe from a fixed point to the deepest probing depth. Using stent to standardize the measurements.

Clinical attachment level

时间窗: Measured at baseline, 6 months and 12 months

According to Ramfjord, clinical parameter measured by a Naber\'s probe. Using stent to standard measurements.

Bleeding on probing

时间窗: Measured at baseline, 6 months and 12 months

According to Ramfjord, the bleeding at each site observed after probing and recorded positive if bleeding was observed within 30 seconds, if not was recorded as negative.

次要结局

  • Radiographic outcome(measured at baseline and 1 year follow up)

研究者

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

Banan Lotfy Mohamed Amer

Assistant lecturer at periodontology department, Principal Investigator, MSC

Tanta University

研究点 (1)

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