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临床试验/ACTRN12613001034729
ACTRN12613001034729尚未招募未知

A prospective split mouth clinical study comparing the bone levels and soft tissue aesthetics of single tooth implants restored using a one abutment one crown at one time concept with implants restored using the traditional multi abutment/ temporary crown to permanent crown concept.

Dr Anand Patel0 个研究点目标入组 12 人开始时间: 2013年9月17日最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Inclusion criteria
  • Healthy males and females over the age of 18 will:
  • *Be informed of the nature of the study and will be given a written informed consent,
  • *Have no significant diseases/ medical conditions during screening,
  • *Be on no regular medical treatment or on medication affecting bone physiology,
  • *Be able to communicate effectively with study personnel,
  • &Have a missing tooth on each side of the one jaw in the antero lateral segments,
  • *Have adequate bone levels (judged by radiographic assessment) to afford an implant based therapy to replace these missing teeth, and
  • *Be keen and motivated to have these missing teeth replaced.

排除标准

  • Exclusion criteria
  • *Any disease or condition which might compromise the haematopoietic, renal, endocrine, pulmonary, central nervous, cardiovascular, immunological, dermatological, gastrointestinal or any other body system.
  • *History of allergic conditions – asthma, urticaria, eczema.
  • *History of autoimmune disorders – lupus erythematosis (SLE).
  • *History of psychiatric disorders.
  • *Pregnancy or not using appropriate means on contraception.
  • *Use of any recreational drugs or a history of drug addiction.
  • *Bisphosphonate therapy.
  • *Patients with uncontrolled dental diseases like caries and periodontitis.
  • *Poor Oral hygiene
  • *Ridge deficiencies that warrant bone augmentation procedure either at or prior to implant placement. The minimum ridge dimension of 7mm width as measured by a ridge caliper or using a cone beam CT scan will be applied as a preliminary criteria. ( Should the subject need an augmentation for implants to be placed and should he/ she meet no other exclusion criteria but meet all inclusion criteria , he/ she can be reassessed for inclusion 6 months after an augmentation procedure ( at patients cost ) ).
  • *Patients lack of availability as and when recalled or attitudes / expectations gauged during interview process will be assessed for eligibility for the study.

研究者

发起方
Dr Anand Patel

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