Onderzoek naar relaties tussen nachtelijk knarsetanden en complicaties rond tandimplantaten.

Completed

Conditions: Inflammation of peri-implant tissues, marginal bone loss, implant technical complications, suprastructure complications, implant mobility, loss of osseointegration.

Registration Number: NL-OMON27266

Lead Sponsor: Academisch Centrum Tandheelkunde Amsterdam (ACTA)

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: Not specified

Target Recruitment: 100

Inclusion Criteria

Planned for treatment with implant-supported fixed suprastructure(s).
- 18 years of age or older.

Exclusion Criteria

- Opposing teeth of implant-supported fixed suprastructure(s) are restored with removable artificial teeth.
- Patients categorized in the classes 3 or higher according to the ASA system for classification of physical status.
- Use of occlusal splint, mandibular repositioning appliance or any other bruxism mitigating device during sleep.
- Active periodontitis at the time of implant placement.
- Known allergy to GrindcareÂ® electrode material.
- Patients with a pacemaker.
- Swollen, infected or inflamed tissues or skin eruptions, e.g. phlebitis, varicose veins etc. in the placement area of the GrindcareÂ® electrode.
- Pregnant women will not be treated with dental implants. Pregnancy after placement of implants will not be a reason to stop participation of the subject in the study.

Study & Design

Study Type: Observational non invasive

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Peri-implant inflammation and implant technical complications (modified gingival index, probing depth, implant mobility, marginal bone height, suprastructure complications, abutment complications, implant fracture, other complications)

Secondary Outcome Measures