Prospective, controlled, clinical cohort study on the use of the MDI® system for the stabilisation of mandibular complete dentures using 4 MDI from IMTEC (3M ESPE) in edentulous patients.

zmk Bern0 个研究点目标入组 20 人开始时间: 2023年12月14日最近更新: 2024年8月19日

适应症

试验速览

暂无简介。

•People/participants who have been edentulous for at least 6 months and have been fitted with sufficient complete dentures for at least 6 weeks. Furthermore, patients must have sufficient bone in the mandible to allow implant placement. The study subjects will not be recruited separately, but will be selected from the clinic's existing patient population: The potential study subjects will be treated with MDI IMTEC implants even if they decline to participate in the study. The study subjects must not fulfil the following exclusion criteria.

•psychologically
•- Participants who are not willing to come to the follow-up appointments
•- Participants who are addicted to alcohol or drugs
•- Participants with pathologically increased dental treatment anxiety
•- Participants who are cognitively incapable of understanding and completing the study questionnaire
•- Uncontrolled diabetes mellitus
•- Post-radiotherapy in the head and neck area
•- Infectious diseases such as active tuberculosis, acute hepatitis, HIV
•- Immunosuppressive drug therapy
•- Osteopathies, e.g. Paget's disease
•- Taking medication that can have a negative effect on bone metabolism, e.g. bisphosphonates
•- General illnesses that do not allow the described course of treatment
•- Pronounced xerostomia
•- Participants with insufficient bone stock for implantation
•- Myoarthropathies
•- Participants with inadequate oral hygiene
•- Participants with untreated or unhealed oral mucosal disease

发起方

zmk Bern