Investigation of the influence of different cements on the retention behavior of implant-supported single crowns and the peri-implant soft tissue. - InKo 2.0

niversitätsklinikum Heidelberg,Poliklinik für Zahnärztliche Prothetik0 个研究点目标入组 30 人开始时间: 2017年3月21日最近更新: 2024年8月19日

适应症

试验速览

暂无简介。

•Prerequisite for the participation of the patients in the clinical trial is the signature of the consent form of the full-year and fully-operational patient. Only subjects who have received a bonelevel implant which is already osseointegrated and does not have any inflammatory signs during the clinical examination are selected. The patient has to be informed about the treatment alternatives, their advantages and disadvantages as well as their costs and have decided against alternative proposals.

•A lack of consent, minority or limited legal capacity leads to the exclusion of patients from the study. No change of the patient's location may be planned. Patients with tissue level implants, pregnant women and breastfeeding mothers, as well as patients with state after radiation in the jaw / facial region or bisphosphonate therapy within the last ten years are also excluded. Patients whose implants already have clinical signs of mucositis or peri-implantitis at the beginning of studies are also not included.

发起方

niversitätsklinikum Heidelberg,Poliklinik für Zahnärztliche Prothetik