Microbial adhesion and biofilm formation on various approved oral implants in situ

• Conditions: K10.9; Disease of jaws, unspecified

• Registration Number: DRKS00031685
• Lead Sponsor: niversitätsklinikum Freiburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-08-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

•Written consent form.
•Age: at least 18 years.
•Good average health as assessed by the investigator.
•Healthy teeth and periodontium.
•Non-smoker

Exclusion Criteria

•Use of mouth rinses or antibiotics in the last 3 months.
•Pregnancy and lactation.
•Participation in another clinical trial, currently or within the last 30 days.
•Gingivitis/periodontitis.
•Smoker.
•Dental caries.
•Previous orthodontic treatment.
•Systemic disease.
•Autoimmune disease
•Infections
•Diabetes
•Previous periodontal treatment.
•Reflux esophagitis
•Drug use

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary endpoint is phenotypic and quantitative microbial characterization of initial microbial adhesion and biofilm formation on various oral implant materials in situ.

Secondary Outcome Measures

Name	Time	Method
The secondary endpoint is the suitability of the implants for clinical use.