Clinical Evaluation of Three Different Universal Adhesives and a Universal Flowable Composite for Restoration of Non-carious Cervical Lesions
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 18
- 主要终点
- Clinical performances of different universal adhesives
研究概览
简要总结
The aim of this randomized, controlled prospective clinical trial is to evaluate and compare the performances of three different universal adhesives using a flowable universal composite resin in the restoration of non-caries cervical lesions over 48-month period.Participants over 18 will be included to the study. Oral hygiene instructions will be given before procedures. All the lesions will be restored by the same clinician who will not participate to the selection of patients for eligibility. Each patient will receive at least three restorations and randomization will be applied using a table of random numbers. All lesions will be cleaned before restoring. Adhesive procedures and restorations will be placed according to manufacturers' recommandation.
The flowable universal composite resin will be placed in bulk and light-cured for 40 seconds. The restorations will be contoured and polished with Optidisc discs (Kerr Coorporation, Orange, CA, USA).
Patients will be recalled at baseline and will be recalled at control periods after placement.
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 (Participant)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •18 years old with 20 teeth under occlusion. They will be required to have at least three NCCLs needed restoration in different teeth. All the NCCLs selected were in similar sizes varying between 1-3 mm.
排除标准
- •Patients with severe periodontal disease, rampant, uncontrolled caries, xerostomia, serious medical problems preventing them from attending review visits, poor gingival health, heavy bruxism and removable partial dentures will not be included in the present study. Also, participiants will be excluded, if they are undergoing bleaching treatment or orthodontic treatment.
研究组 & 干预措施
Group CU (Clearfil Universal)
Clearfil Univesal Bond (Kuraray Dental, New York, United States of America), adhesive system
干预措施: Clearfil Univesal Bond (Device)
Group IU (Ibond Universal)
IBond Universal (Heraeus Kulzer GmbH, Hanau, Germany), adhesive system
干预措施: IBond Universal (Device)
Group GP (G-Premio)
G-Premio Bond (GC Coorporation, Tokyo, Japan), adhesive system
干预措施: G-Premio Bond (Device)
结局指标
主要结局
Clinical performances of different universal adhesives
时间窗: Two years
Two year results according to USPHS criteria
次要结局
未报告次要终点
研究者
Dr. Fatma Dilşad Öz
Principal Investigator
Hacettepe University