In vivo analysis of undisturbed biofilm formation, composition and growth on implant abutment restorative materials using a novel implant-supported biofilm device

The University of Sydney0 个研究点目标入组 5 人开始时间: 2022年5月17日最近更新: 2022年6月6日

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试验速览

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•The inclusion criteria for the potential participants include:
•Adults aged 21 years and more that are suitable for dental implants treatment or have received already an implant that needs to be restored in the posterior region (non-esthetic sites).
•Medically healthy without any active dental or periodontal diseases.
•Good oral hygiene assessed by a full-mouth bleeding and plaque score.
•Participants need to be willing to provide informed consent and willing to participate and comply with the study requirements.

•Participants that are not eligible for dental implant treatment. Absolute contraindications to dental implant treatment include recent myocardial infarction and cerebrovascular accident, valvular prosthesis surgery, immunosuppression, bleeding issues, active treatment of malignancy, drug abuse, psychiatric illness, and intravenous bisphosphonate use (Hwang & Wang, 2006).
•Participants with failing/compromised implants or peri-implantitis.
•Implant sites located in aesthetic zones, and sites that require tissue augmentation / grafting.
•Pregnant/lactating patients
•Antibiotic therapy in the last 3 months.
•Completely edentulous patients

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