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临床试验/NCT02905838
NCT02905838已完成不适用

Comparison of the Esthetic and Clinical Performance of Implant Supported All Ceramic Crowns Using Two Different Ceramic Abutment Types

University of Bern0 个研究点目标入组 40 人开始时间: 2010年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
主要终点
Change in Aesthetic scores: Pink Esthetic Score / White Esthetic Score (PES WES) baseline, 6 months, 1, 3, 5 years performed by 2 independent observers in each center

研究概览

简要总结

To assess and compare the esthetic outcome and clinical performance of anterior maxillary all ceramic implant single crowns based either on prefabricated zirconia abutment veneered with pressed ceramics or on a CAD/CAM (computer-aided design and computer-aided manufacturing) CARES® abutment veneered with hand build-up technique.

Participants will be recruited from the patient population who has previously received dental implant treatment, received a provisional restoration and met the inclusion and exclusion criteria according to the study protocol. After final impression, patients will be randomised into Group A (prefabricated anatomic abutments ): one-piece screw retained single crown using a press technique (fluorapatite glass-ceramic, e.max ZirPress) with cut-back technique or Group B (CAD/CAM CARES® abutments): one- piece screw retained single crown with a hand build-up technique (fluorapatite veneering ceramic, e.max Ceram). One week after final restoration (base line visit) the primary and secondary outcome parameters will be assessed. The patients will be followed up to 5 years after final restoration.

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

  • Subjects must have voluntarily signed the informed consent form before any study-related action
  • Males and females with at least 18 years of age
  • Single tooth gaps in the anterior maxilla position 14-24 (FDI)
  • Successfully osseointegrated single tooth implant inserted at least 16 weeks after tooth extraction
  • Full mouth plaque index according to O'Leary ≤ 25%
  • Implant axis compatible with transocclusal screw retention (screw access palatal of incisal edges)

排除标准

  • Systemic disease that would interfere with dental implant therapy
  • Any contraindications for oral surgical procedures
  • History of local irradiation therapy
  • Patients who smoke >10 cigarettes per day or tobacco equivalents or chew tobacco
  • Subjects who had undergone administration of any investigational device within 30 days of enrolment in the study
  • Conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of non-compliance
  • Physical or mental handicaps that would interfere with the ability to perform adequate oral hygiene
  • Pregnant or breastfeeding women
  • Existing implants in the adjacent position
  • Removable dentures or un-restored tooth gaps in the opposing dentition
  • Patients with inadequate oral hygiene or unmotivated for adequate home care
  • Probing pocket depth of ≥ 4 mm on one of the teeth immediately adjacent to the dental implant site
  • Lack of primary stability of the implant
  • Inappropriate implant position for the prosthetic requirements
  • Major simultaneous augmentation procedures
  • Insufficient stability of the implant
  • Screw access position located too close to the planned incisal edge
  • Need of angled abutment due to prosthetic malposition of the implant
  • Height of the abutment is less than 65% of the height of the complete restoration
  • Severe bruxing or clenching habits

结局指标

主要结局

Change in Aesthetic scores: Pink Esthetic Score / White Esthetic Score (PES WES) baseline, 6 months, 1, 3, 5 years performed by 2 independent observers in each center

时间窗: baseline, 6 months, 1 year, 3 years, 5 years

次要结局

  • Change in Clinical Peri-implant Measurements(baseline, 6 months, 1 year, 3 years, 5 years)
  • Implant Success(baseline, 6 months, 1 year, 3 years, 5 years)
  • Survival Rate(baseline, 6 months, 1 year, 3 years, 5 years)
  • Cast Analysis(baseline, 6 months, 1 year, 3 years, 5 years)
  • Number of Technical Complications of the Implant Crown(baseline, 6 months, 1 year, 3 years, 5 years)

研究者

申办方类型
Other
责任方
Sponsor

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