跳至主要内容
临床试验/NCT03384004
NCT03384004Unknown不适用

Effect of Apical Negative Pressure Irrigation System at Cleaning Lateral Canals and Reduction of Periapical Lesions After Endodontic Therapy

KaVo Kerr2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2017年11月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
KaVo Kerr
入组人数
60
试验地点
2
主要终点
Change from baseline - Area of the lateral canal filled at 6 months and 1 year

研究概览

简要总结

The aim of the present study is to assess with PA x-rays and CBCT scans the volumetric changes in periapical radiolucencies in endodontically treated teeth 1 year after endodontic treatment and evaluate how well the lateral canals are filled after irrigation with the new generation of negative irrigation pressure unit with and without the ultrasonic irrigation.

详细描述

This is a single center, prospective clinical study conducted in patients who present for routine endodontic therapy. The study has been reviewed and approved by the Institutional Review Board (Ethics Committee) Aspire IRB located at Santee, CA. The clinical investigator will treat patients who present with radiographic evidence of periapical pathology and will randomize the subjects to either negative pressure irrigation system treatment (EndoVac Pure) with ultrasonic irrigation or negative pressure irrigation system treatment (Endovac Pure) without ultrasonic irrigation. All other aspects of the treatment (access, instrumentation and obturation will be according to clinicians conventional clinical judgment. Subjects will have a pre-treatment PA x-ray and CBCT scan before treatment, a PA x-ray at six months and a CBCT scan at one year post-treatment.

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
None

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

  • Demonstrates understanding of the study and willingness to participate as evidenced by voluntary written informed consent and has received a signed and dated copy of the informed consent form.
  • Aged at least 18 years.
  • Understands and is willing, able and likely to comply with all study procedures and restrictions.
  • Good general and mental health in the opinion of the investigator or medically qualified designee;
  • No clinically significant and relevant abnormalities of medical history or oral examination;
  • Absence of any condition that would impact on the subject's safety or wellbeing or affect the individual's ability to understand and follow study procedures and requirements.
  • Single or multi rooted-canal teeth diagnosed with pulp necrosis and symptomatic/ asymptomatic apical periodontitis as tested with routine diagnostics.
  • Radiographic evidence of periapical lesion.

排除标准

  • Women who are known to be pregnant or who are intending to become pregnant over the duration of the study.
  • Women who are breast-feeding.
  • Pre-existing oral irritations. b) Recent (within 30 days) gingival/oral surgery. c) Any clinically significant or relevant oral abnormality.
  • Known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients.
  • Any subject requiring re-treatment.

研究组 & 干预措施

Irrigation Technique 1

Experimental

Patients randomized into this group will be treated using EndoVac Pure followed by Ultrasonic Irrigation.

干预措施: Irrigation Technique 1 (Device)

Irrigation Technique 2

Experimental

Patients randomized into this group will be treated using EndoVac Pure only.

干预措施: Irrigation Technique 2 (Device)

结局指标

主要结局

Change from baseline - Area of the lateral canal filled at 6 months and 1 year

时间窗: 6 months and 1 year post treatment

The study will also measure the area occupied by the filling material inside the lateral canal in relation to its entire area in mm²).

Change from baseline - Size of the lesion in the lateral canals at 1 year

时间窗: 1 year after endodontic therapy

Evaluate the efficacy of EndoVac Pure at cleaning lateral canals as evidenced by post-treatment CBCT scans. CBCT images will be analyzed and the size of the lesion will be measured and will be evaluated.

Change from baseline - Length of lateral canal filled at 6 months and 1 year

时间窗: 6 months and 1 year post treatment

The study will also evaluate how well the lateral canals are filled after irrigation with the new generation of negative irrigation pressure unit with and without the ultrasonic irrigation The amount of filling material visualized in each lateral canal will be calculated and expressed as a percentage of linear extension (length of the lateral canal that was filled, in relation to its entire length in mm).

次要结局

  • Change from baseline - Periapical radiographic healing(6 months and 1 year after endodontic therapy)

研究者

发起方
KaVo Kerr
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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