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临床试验/NCT02867982
NCT02867982Unknown不适用

Influence of Soft Tissue Thickness and Insertion Depth of Platform Switched Implants on Crestal Bone Level Alteration

Beijing University Health Science Center0 个研究点目标入组 36 人开始时间: 2016年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
36
主要终点
Changes of marginal bone levels of dental implant

研究概览

简要总结

This is a two-year prospective randomized clinical study to to evaluate whether the gingival thickness and insertion depth of dental implants have any influence on marginal bone levels changes around platform switched implants.

详细描述

Patient selection: Patients at the Department of Oral Implantology, Peking University School and Hospital of stomatology, Bei Jing, China, who seek for implant restoration for two continous posterior teeth are potentially recruited. Inclusion criteria are generally healthy (ASA score I), non-smoking, periodontally healthy, and sufficient bone volume to place an implant without augmentation procedure. Patients were excluded in cases of medical and/or psychiatric contraindications, local infection, pregnancy or lactating, poor oral hygiene, tissue deficiency, or not willing to participate in this study.

Randomization: The two implant sites of each subject are randomly assigned to two different group with a predefined randomization tables. In order to reduce the chance of unfavorable splits between groups in terms of key prognostic factors,the randomization process will take into account the following variables: patient's gender, age, presence of adjacent teeth, distal extension sites and site location in the dental arch. Assignment will perform using a sealed envelope.

Surgical protocol: Before the surgical procedure, prophylactic antibiotics of 1g amoxicillin will prescribed to the patient 1 h before surgery, and continued with 2 g/day for 6 days. After crestal incision, full thickness buccal flap was raised, whereas lingual part was not elevated. Thickness of soft tissues was measured with 1.0-mm marked periodontal probe on the top of bone crest in the center of the two future implant sites. This ensured direct visibility of mucosal thickness during measurement. After measurements, full-thickness lingual flap is raised and subsequent implant osteotomy is finished, Two dental implants (Dentsply Implants Manufacturing GmbH, Mannheim, Germany) with diameter of 3.5 mm are ready to torch into the bone cavities. In one site (group 1), the platform of implants are placed at the crestal level (flush to the alveolar ridge) . In the other site (group 2), the implants are placed 1mm below the alveolar ridge. narrow healing abutment are connected to all the implants. The flap are repositioned and closed with interrupted single sutures. Implants are allowed for a un-submerged healing. 3 month after healing, the implant level impressions are taken, splinted restorations of two neighbouring posterior teeth are delivered 2 weeks later.

Radiographic and Clinical Examination: All the patients are required for recall visit at 3, 6,12 months and 2 years post surgery. A digital peri-apical radiograph was taken at the 1 year and 2year follow-up examination for bone level evaluation using a film holder to aim the x-ray beam perpendicular to the implant threads, and the implant length is used as calibration for the measurement. Using a image analysis software (ImageJ, version 1.47, NIH, Bethesda, MD, USA), the investigators are able to have an accurate assessment of the crest of bone and to analyze the bone changes over period of time. Bone loss was defined as a positive value and bone gain as a negative one. Mean values, standard deviations, and maximum and minimum values were calculated. Furthermore, periodontal parameters [bleeding on probing (BOP), probing pocket depth (PPD), modified plaque index on adjacent teeth and implants] were assessed.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • lose of two posterior teeth more than 3 months
  • generally healthy (ASA score I)
  • non-smoking
  • periodontally healthy
  • sufficient bone volume to place an implant without augmentation procedure

排除标准

  • medical and/or psychiatric contraindication to dental implant restoration
  • local infection
  • pregnancy or lactating
  • poor oral hygiene
  • tissue deficiency

研究组 & 干预措施

Subcrestal

Other

implants that are placed below the alveolar ridge

干预措施: Subcrestal implant placement (Procedure)

Subcrestal

Other

implants that are placed below the alveolar ridge

干预措施: prophylactic antibiotics (Drug)

Subcrestal

Other

implants that are placed below the alveolar ridge

干预措施: dental implant (Device)

Subcrestal

Other

implants that are placed below the alveolar ridge

干预措施: x-ray examination (Radiation)

Paracrestal

Other

implants that are placed flush to the alveolar ridge

干预措施: Paracrestal implant placement (Procedure)

Paracrestal

Other

implants that are placed flush to the alveolar ridge

干预措施: prophylactic antibiotics (Drug)

Paracrestal

Other

implants that are placed flush to the alveolar ridge

干预措施: dental implant (Device)

Paracrestal

Other

implants that are placed flush to the alveolar ridge

干预措施: x-ray examination (Radiation)

结局指标

主要结局

Changes of marginal bone levels of dental implant

时间窗: 3 months, 6 months, 1 year and 2 years post intervention (implant surgery)

Mesial and distal marginal bone level alterations at different time point compared with the base line. Marginal bone levels were measured with an image analysis software to the accuracy of 0.01 mm and the implant length is used as calibration for the measurement.

次要结局

  • Bleeding on probing(BOP)(3 months, 6 months, 1 year and 2 years post intervention (implant surgery))
  • modified plaque index(PI)(3 months, 6 months, 1 year and 2 years post intervention (implant surgery))
  • Probing pocket depth(PPD)(3 months, 6 months, 1 year and 2 years post intervention (implant surgery))

研究者

发起方
Beijing University Health Science Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jiang Xi

Dr.

Beijing University Health Science Center

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