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临床试验/NCT04757753
NCT04757753进行中(未招募)不适用

Evaluation of the Efficacy Rate of Endodontic Treatment at 2 Years After Root Canal Filling With a Ready-to-use Root Canal Sealer PA1704 Versus BioRoot™ RCS: a Randomized Controlled Trial

Septodont9 个研究点 分布在 2 个国家目标入组 160 人开始时间: 2020年11月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Septodont
入组人数
160
试验地点
9
主要终点
Efficacy Rate of Root Canal Obturation

研究概览

简要总结

The study design is a multicentric randomized controlled non-inferiority trial. 160 subjects (teeth) requiring a primary or a secondary root canal treatment will be enrolled in 2 groups (80 in each group). The aim of the study is to assess the efficacy rate and the safety 2 years after root canal obturation undertaken using a ready-to-use calcium silicate sealer (PA1704) compared to the control calcium silicate sealer BioRoot™ RCS.

Procedures of root canal treatment will be conventional and standardized for all investigational centers. The canals will be cleaned, shaped and then obturated using a calcium silicate sealer (the ready to use sealer PA1704 or BioRoot™ RCS) with a single cone technique or cold lateral condensation of gutta-percha. Follow-up assessments will be conducted at 6, 12 and 24 months in both groups. The performance and safety of the sealer PA1704 will also be evaluated at 3.5 and 5 years after surgery. Retroalveolar radiographs will be taken at each study visit. The preoperative, postoperative and follow-up clinical and radiographic data will be analyzed.

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)

盲法说明

Blinding will be done to the assessors who analyzed radiographs to reduce bias to healing assessment.

入排标准

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

入选标准

  • Adult male or female (age ≥ 18 years)
  • Patient requiring a primary or a secondary root canal obturation on a single or multi-rooted tooth,
  • Patient geographically stable who can be followed by the same investigator site for 2 years,
  • Informed consent signed,
  • Patient with social protection

排除标准

  • Patient with one or more documented contraindication to endodontic treatment,
  • Contraindication to the use of calcium silicate root canal sealer, such as an immature tooth or a known hypersensitivity to one component of the sealer formula,
  • Endodontic treatment on tooth with calcified root canal assessed radiographically,
  • Endodontic treatment on tooth with suspected perforation,
  • Patient with an uncontrolled systemic disease such as diabetes or thyroid disorders, or with an immunocompromised condition or who has undergone radiation therapy to the jaw.
  • Patient suffering from uncontrolled active periodontitis, not supported
  • Participation to another interventional clinical study at the same time,
  • Vulnerable subjects referred to in articles L.1121-5 to 8 and L.1122-1-2 of the Public Health Code and article 66 of Regulation (EU) 2017/745 on medical devices are excluded from the investigation (such as known pregnancy or lactation, patients with legal protection).

研究组 & 干预措施

ready-to-use root canal sealer: PA1704

Experimental

PA1704 is used in combination with gutta percha points for the permanent obturation of root canals.

干预措施: ready-to-use root canal sealer: PA1704 (Device)

root canal sealer: BioRoot™ RCS

Other

BioRoot™ RCS is used in combination with gutta percha points for the permanent obturation of root canals.

干预措施: root canal sealer: BioRoot™ RCS (Device)

结局指标

主要结局

Efficacy Rate of Root Canal Obturation

时间窗: 24 months post-treatment

Efficacy rate of root canal obturation using clinical and radiological criteria. A successfull treatment is defined in this study, based on some loose criteria, as: a functional tooth with no lesion on the radio, or a functional tooth with a size reduction of the lesion on the radio, or a functional tooth with a lesion size stabilisation.

次要结局

  • Efficacy Rate of Root Canal Obturation(6 months post-treatment)
  • Radiological Evaluation of the Canal Obturation(24-months post-treatment)
  • Postoperative Pain(Before endodontic treatment*; before session#2 initiation**; T0 (after canal obturation); 12; 24; 48; & 72h; 7 days after endodontic treatment. *Evaluation on same day for 1-session treatment; up to 18 days before if 2 sessions needed. **On same day.)
  • Use of Oral Pain Treatment(From Day 0 to Day 7)

研究者

发起方
Septodont
申办方类型
Industry
责任方
Sponsor

研究点 (9)

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