跳至主要内容
临床试验/DRKS00033851
DRKS00033851尚未招募不适用

Clinical and radiographic effects of TiUltra after prosthetic restoration - a practice-based observational study - non Xeal_TiUltra

ZahnMedizinCenter-Anhalt0 个研究点目标入组 24 人开始时间: 2024年3月22日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Mentally healthy adults, i.e. patients capable of giving consent
  • - Good general health (ASA = 2)
  • a.Diabetes mellitus should be well controlled (HbA1c < 7)
  • b.Smoking = 20 cigarettes / day
  • c.No alcohol or drug abuse
  • - No pathology of the bone metabolism
  • - Patients with periodontitis should be successfully treated, i.e. no remaining periodontal infection as far as possible
  • - Good oral hygiene and compliance, i.e. plaque level (full-mouth plaque score, FMPS) < 25% and bleeding level after probing (full-mouth bleeding on probing score, FMBS) < 25%
  • - A 3D radiological bone volume (possibly after augmentative procedures such as sinus lift) must be available for insertion of the planned implants.
  • - Patient and anatomical conditions must correspond to the instructions for use of the implants to be used (Nobel Parallel Conical Connection, TiUltra surface).
  • - Edentulous areas must be suitable for the planned implant-supported restoration.
  • - Sufficiently keratinised peri-implant mucosa.
  • - Tooth removal should generally have taken place three months previously.
  • - Existing opposing dentition
  • - Patients must be prepared to adhere to a prevention concept (supportive therapy, UT). This is a routine protocol.
  • - Written informed consent for participation in this study

排除标准

  • - Pregnant and breastfeeding patients
  • - Taking antiresorptives
  • - Patients with a known titanium allergy
  • - Patients with CMD symptoms

研究者

发起方
ZahnMedizinCenter-Anhalt

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